RESTASIS ® ophthalmic emulsion is indicated to increase tear production in patients whose tear production is presumed to be suppressed due to ocular inflammation associated with keratoconjunctivitis sicca. Increased tear production was not seen in patients currently taking topical anti-inflammatory drugs or using punctal plugs.
Invert the unit dose vial a few times to obtain a uniform, white, opaque emulsion before using. Instill one drop of RESTASIS ® ophthalmic emulsion twice a day in each eye approximately 12 hours apart. RESTASIS ® can be used concomitantly with artificial tears, allowing a 15 minute interval between products. Discard vial immediately after use.
Sterile, Preservative-Free
RESTASIS® (cyclosporine ophthalmic emulsion) 0.05% contains a topical immunomodulator with anti-inflammatory effects. Cyclosporine's chemical name is Cyclo[[(E)-(2S,3R,4R)-3-hydroxy-4-methyl-2-(methylamino)-6-octenoyl]-L-2-aminobutyryl-N-methylglycyl-N-methyl-L-leucyl-L-valyl-N-methyl-L-leucyl-L-alanyl-D-alanyl-N-methyl-L-leucyl-N-methyl-L-leucyl-N-methyl-L-valyl] and it has the following structure:
Structural Formula
Cyclosporine is a fine white powder. RESTASIS ® appears as a white opaque to slightly translucent homogeneous emulsion. It has an osmolality of 230 to 320 mOsmol/kg and a pH of 6.5-8.0. Each mL of RESTASIS ® ophthalmic emulsion contains: Active: cyclosporine 0.05%. Inactives: glycerin; castor oil; polysorbate 80; carbomer copolymer type A; purified water; and sodium hydroxide to adjust pH.
Cyclosporine is an immunosuppressive agent when administered systemically.
In patients whose tear production is presumed to be suppressed due to ocular inflammation associated with keratoconjunctivitis sicca, cyclosporine emulsion is thought to act as a partial immunomodulator. The exact mechanism of action is not known.
Blood cyclosporin A concentrations were measured using a specific high pressure liquid chromatography-mass spectrometry assay. Blood concentrations of cyclosporine, in all the samples collected, after topical administration of RESTASIS ® 0.05%, BID, in humans for up to 12 months, were below the quantitation limit of 0.1 ng/mL. There was no detectable drug accumulation in blood during 12 months of treatment with RESTASIS ® ophthalmic emulsion.
Four multicenter, randomized, adequate and well-controlled clinical studies were performed in approximately 1200 patients with moderate to severe keratoconjunctivitis sicca. RESTASIS ® demonstrated statistically significant increases in Schirmer wetting of 10 mm versus vehicle at six months in patients whose tear production was presumed to be suppressed due to ocular inflammation. This effect was seen in approximately 15% of RESTASIS ® ophthalmic emulsion treated patients versus approximately 5% of vehicle treated patients. Increased tear production was not seen in patients currently taking topical anti-inflammatory drugs or using punctal plugs.
No increase in bacterial or fungal ocular infections was reported following administration of RESTASIS ®.
RESTASIS® ophthalmic emulsion is indicated to increase tear production in patients whose tear production is presumed to be suppressed due to ocular inflammation associated with keratoconjunctivitis sicca. Increased tear production was not seen in patients currently taking topical anti-inflammatory drugs or using punctal plugs.
RESTASIS® is contraindicated in patients with active ocular infections and in patients with known or suspected hypersensitivity to any of the ingredients in the formulation.
RESTASIS® ophthalmic emulsion has not been studied in patients with a history of herpes keratitis.
General: For ophthalmic use only.
The emulsion from one individual single-use vial is to be used immediately after opening for administration to one or both eyes, and the remaining contents should be discarded immediately after administration.
Do not allow the tip of the vial to touch the eye or any surface, as this may contaminate the emulsion.
RESTASIS® should not be administered while wearing contact lenses. Patients with decreased tear production typically should not wear contact lenses. If contact lenses are worn, they should be removed prior to the administration of the emulsion. Lenses may be reinserted 15 minutes following administration of RESTASIS ® ophthalmic emulsion.
Systemic carcinogenicity studies were carried out in male and female mice and rats. In the 78-week oral (diet) mouse study, at doses of 1, 4, and 16 mg/kg/day, evidence of a statistically significant trend was found for lymphocytic lymphomas in females, and the incidence of hepatocellular carcinomas in mid-dose males significantly exceeded the control value.
In the 24-month oral (diet) rat study, conducted at 0.5, 2, and 8 mg/kg/day, pancreatic islet cell adenomas significantly exceeded the control rate in the low dose level. The hepatocellular carcinomas and pancreatic islet cell adenomas were not dose related. The low doses in mice and rats are approximately 1000 and 500 times greater, respectively, than the daily human dose of one drop (28 μL) of 0.05% RESTASIS ® BID into each eye of a 60 kg person (0.001 mg/kg/day), assuming that the entire dose is absorbed.
Cyclosporine has not been found mutagenic/genotoxic in the Ames Test, the V79-HGPRT Test, the micronucleus test in mice and Chinese hamsters, the chromosome-aberration tests in Chinese hamster bone-marrow, the mouse dominant lethal assay, and the DNA-repair test in sperm from treated mice. A study analyzing sister chromatid exchange (SCE) induction by cyclosporine using human lymphocytes in vitro gave indication of a positive effect (i.e., induction of SCE).
No impairment in fertility was demonstrated in studies in male and female rats receiving oral doses of cyclosporine up to 15 mg/kg/day (approximately 15,000 times the human daily dose of 0.001 mg/kg/day) for 9 weeks (male) and 2 weeks (female) prior to mating.
Pregnancy category C.
Teratogenic Effects: No evidence of teratogenicity was observed in rats or rabbits receiving oral doses of cyclosporine up to 300 mg/kg/day during organogenesis. These doses in rats and rabbits are approximately 300,000 times greater than the daily human dose of one drop (28 μL) 0.05% RESTASIS ® BID into each eye of a 60 kg person (0.001mg/kg/day), assuming that the entire dose is absorbed.
Non-Teratogenic Effects: Adverse effects were seen in reproduction studies in rats and rabbits only at dose levels toxic to dams. At toxic doses (rats at 30 mg/kg/day and rabbits at 100 mg/kg/day), cyclosporine oral solution, USP, was embryo- and fetotoxic as indicated by increased pre- and postnatal mortality and reduced fetal weight together with related skeletal retardations. These doses are 30,000 and 100,000 times greater, respectively than the daily human dose of one drop (28 μL) of 0.05% RESTASIS ® BID into each eye of a 60 kg person (0.001 mg/kg/day), assuming that the entire dose is absorbed. No evidence of embryofetal toxicity was observed in rats or rabbits receiving cyclosporine at oral doses up to 17 mg/kg/day or 30 mg/kg/day, respectively, during organogenesis. These doses in rats and rabbits are approximately 17,000 and 30,000 times greater, respectively, than the daily human dose.
Offspring of rats receiving a 45 mg/kg/day oral dose of cyclosporine from Day 15 of pregnancy until Day 21 postpartum, a maternally toxic level, exhibited an increase in postnatal mortality; this dose is 45,000 times greater than the daily human topical dose, 0.001 mg/kg/day, assuming that the entire dose is absorbed. No adverse events were observed at oral doses up to 15 mg/kg/day (15,000 times greater than the daily human dose).
There are no adequate and well-controlled studies of RESTASIS ® in pregnant women. RESTASIS ® should be administered to a pregnant woman only if clearly needed.
Cyclosporine is known to be excreted in human milk following systemic administration but excretion in human milk after topical treatment has not been investigated. Although blood concentrations are undetectable after topical administration of RESTASIS ® ophthalmic emulsion, caution should be exercised when RESTASIS ® is administered to a nursing woman.
The safety and efficacy of RESTASIS ® ophthalmic emulsion have not been established in pediatric patients below the age of 16.
No overall difference in safety or effectiveness has been observed between elderly and younger patients.
The most common adverse event following the use of RESTASIS ® was ocular burning (17%).
Other events reported in 1% to 5% of patients included conjunctival hyperemia, discharge, epiphora, eye pain, foreign body sensation, pruritus, stinging, and visual disturbance (most often blurring).
Invert the unit dose vial a few times to obtain a uniform, white, opaque emulsion before using. Instill one drop of RESTASIS ® ophthalmic emulsion twice a day in each eye approximately 12 hours apart. RESTASIS ® can be used concomitantly with artificial tears, allowing a 15 minute interval between products. Discard vial immediately after use.
RESTASIS® ophthalmic emulsion is packaged in single use vials. Each vial contains 0.4 mL fill in a 0.9 mL LDPE vial; 30 vials are packaged in a polypropylene tray with an aluminum peelable lid. The entire contents of each tray (30 vials) must be dispensed intact. RESTASIS ® is also provided in a 60 count (2 x 30) package (one month supply) that must be dispensed intact.
30 Vials 0.4 mL each - NDC 54868-4793-1
Storage: Store RESTASIS ® ophthalmic emulsion at 15 - 25° C (59 - 77° F).
KEEP OUT OF THE REACH OF CHILDREN.
Rx Only
Revised: 02/2010
© 2010 Allergan, Inc.
Irvine, CA 92612, U.S.A.
® marks owned by Allergan, Inc.
U.S. Patent 5,474,979
Made in the U.S.A.
71876US14B
Relabeling of "Additional" bar code label by:
Physicians Total Care, Inc.
Tulsa, OK 74146
NDC 54868-4793-1
Restasis
(Cyclosporine Ophthalmic Emulsion) 0.05%
30 Single-Use Vials (0.4 mL each)
Each mL contains: Active: cyclosporine 0.05% Inactives: glycerin; castor oil; polysorbate 80; carbomer copolymer type A; purified water; and sodium hydroxide to adjust the pH. Usual Dosage: Twice daily approximately 12 hours apart. Invert the vial before using. Use immediately after opening and then discard.
Note: Store at 15 - 25° C (59 - 77° F). Store vials in the thermoformed tray until use. The entire contents of each package (60 vials) must be dispensed intact.
Rx only| RxCUI | RxNorm string | TTY | SPL version |
|---|---|---|---|
| 2572292 | cycloSPORINE 0.05 % in 0.4 ML Ophthalmic Emulsion | PSN | 1 |
| 2572293 | Restasis 0.05 % in 0.4 ML Ophthalmic Emulsion | PSN | 1 |
| 2572293 | 0.4 ML cyclosporine 0.5 MG/ML Ophthalmic Suspension [Restasis] | SBD | 1 |
| 2572292 | 0.4 ML cyclosporine 0.5 MG/ML Ophthalmic Suspension | SCD | 1 |
| 2572293 | 0.4 ML Restasis 0.5 MG/ML Ophthalmic Suspension | SY | 1 |
| 2572292 | cyclosporine 0.05 % per 0.4 ML Ophthalmic Emulsion | SY | 1 |
| 2572292 | cyclosporine 0.5 MG/ML per 0.4 ML Ophthalmic Emulsion | SY | 1 |
| 2572293 | Restasis 0.05 % per 0.4 ML Ophthalmic Suspension | SY | 1 |
| Class | Version | Type | Effective |
|---|---|---|---|
| CYCLOSPORINE Pharmacologic Class Indexing | 3 | Indexing - Pharmacologic Class | 20180813 |
| Product concept | Relation | Version | Effective |
|---|---|---|---|
| 1be408a0-e15a-4092-b35e-4e294e65196f | Product name | 3 | 20240216 |
| b3fdee3e-0c46-442f-aad5-aa71941d5621 | Product name | 1 | 20231023 |
| 78fb0708-fce5-decd-6611-5a9fbe3e3dec | Product name | 3 | 20230327 |
| 54840517-000d-4fcb-b976-a6ddd102faa0 | Product name | 1 | 20220120 |
| a5ba3bd0-8411-4005-ac3b-a41d8ee0633a | Product name | 1 | 20181029 |
| b1c0d609-8b97-06ee-2cd0-5652a4b1d019 | Product name | 1 | 20140508 |
| NDC | Effective | Action | Document | Indexing SPL | Related label |
|---|---|---|---|---|---|
| 54868-4793-1 | 2019-09-24 | C162847 | 48780-1 | 9350213a-472d-c013-e053-90daa90a1393 | RESTASIS ® (cyclosporine ophthalmic emulsion) 0.05% |
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 54868-4793-1 | RESTASIS | 30 in 1 TRAY | EMULSION | 30 | 1 | |
| 54868-4793-1 | RESTASIS | 0.4 mL in 1 VIAL, SINGLE-DOSE | EMULSION | 0.4 | 1 |
| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|---|---|---|---|
| 54868-4793 | RESTASIS (CYCLOSPORINE) EMULSION [PHYSICIANS TOTAL CARE, INC.] | 1 | 2 package rows | 20110630_8227ca35-77c1-4a08-87a3-7dcefef39bc5.zip |
| Package NDC | Billing unit | Product NDC | DailyMed indexing SPL | SPL version | Effective |
|---|---|---|---|---|---|
| 54868-4793-1 | EA - Each | 54868-4793 | 6a214aee-61b4-477d-be77-1057f2fde878 | 1 | 2012-07-24 |
| 0023-9163-30 | EA - Each | 0023-9163 | 499f317b-fbe1-417b-9a78-51eb2a931c52 | 1 | 2012-07-24 |
| 0023-9163-60 | EA - Each | 0023-9163 | ba8da38d-8626-4f4d-b00e-0c18f8222f3a | 1 | 2012-07-24 |
| Ingredient | Type | UNII | SPL version | Uploaded |
|---|---|---|---|---|
| CYCLOSPORINE | ACTIVE INGREDIENT | 83HN0GTJ6D | 1 | |
| CYCLOSPORINE | ACTIVE MOIETY | 83HN0GTJ6D | 1 | |
| CARBOMER COPOLYMER TYPE A | INACTIVE INGREDIENT | 71DD5V995L | 1 | |
| CASTOR OIL | INACTIVE INGREDIENT | D5340Y2I9G | 1 | |
| GLYCERIN | INACTIVE INGREDIENT | PDC6A3C0OX | 1 | |
| POLYSORBATE 80 | INACTIVE INGREDIENT | 6OZP39ZG8H | 1 | |
| SODIUM HYDROXIDE | INACTIVE INGREDIENT | 55X04QC32I | 1 | |
| WATER | INACTIVE INGREDIENT | 059QF0KO0R | 1 |
Every source-derived product name is available through these pages.
| Product NDC | Package NDC |
|---|---|
| 54868-4793 | 54868-4793-1 |
| 0023-9163 |
Every source-derived ingredient row is available through these pages.
| Name | UNII | Kind |
|---|---|---|
| CYCLOSPORINE | 83HN0GTJ6D | ACTIB |
| GLYCERIN | PDC6A3C0OX | IACT |
| CASTOR OIL | D5340Y2I9G | IACT |
| POLYSORBATE 80 | 6OZP39ZG8H | IACT |
| CARBOMER COPOLYMER TYPE A | 71DD5V995L | IACT |
| WATER | 059QF0KO0R | IACT |
| SODIUM HYDROXIDE | 55X04QC32I | IACT |
Inactive Ingredient Database values describe FDA-listed use contexts. The match method and ambiguity count are shown because ingredient names, routes, and dosage forms are not always unique. Browse recovered IID releases and source provenance.
| DailyMed ingredient | IID ingredient | UNII | Dosage form / route | Potency | Maximum daily exposure | Match |
|---|---|---|---|---|---|---|
| CASTOR OIL | CASTOR OIL | D5340Y2I9G | EMULSION / OPHTHALMIC | 32 mg | ||
| POLYSORBATE 80 | POLYSORBATE 80 | 6OZP39ZG8H | EMULSION / OPHTHALMIC | 26 mg | ||
| CARBOMER COPOLYMER TYPE A | CARBOMER COPOLYMER TYPE A (ALLYL PENTAERYTHRITOL CROSSLINKED) | 71DD5V995L | EMULSION / OPHTHALMIC | 0.05 %w/v | ||
| SODIUM HYDROXIDE | SODIUM HYDROXIDE | 55X04QC32I | EMULSION / OPHTHALMIC | 0.02 %w/v | ||
| GLYCERIN | GLYCERIN | PDC6A3C0OX | EMULSION / OPHTHALMIC | 3 mg |
All distinct exact application/product contexts derived from this label’s complete NDC list are paginated below.
| Application-product | Trade name | Ingredient | Strength | Dosage form / route | TE codes | RLD / RS | Approval date |
|---|---|---|---|---|---|---|---|
| N050790-001 | RESTASIS | CYCLOSPORINE | 0.05% | EMULSION / OPHTHALMIC | AB | RLD, RS | 2002-12-23 |
| N050790-002 | RESTASIS MULTIDOSE | CYCLOSPORINE | 0.05% | EMULSION / OPHTHALMIC | RLD, RS | 2016-10-27 |
| Application-product | TE code |
|---|---|
| N050790-001 | AB |
| Application-product | Patent | Expiration | Use code | Coverage / status | Submission date |
|---|---|---|---|---|---|
| N050790-002 | 8292129 | 2031-02-25 | Drug product, Delist requested | 2017-06-26 | |
| N050790-002 | 8561859 | 2032-04-16 | Drug product, Delist requested | 2017-06-26 | |
| N050790-002 | 9676525 | 2034-02-07 | Drug product, Delist requested | 2017-06-26 | |
| N050790-002 | 9669974 | 2034-05-11 | Drug product, Delist requested | 2017-06-26 |
Observed FDA ZIP history: Each table is queried independently by exact application/product key from successfully parsed Orange Book snapshots. Capture times identify archived source observations; absence or a change between snapshots is not inferred. FDA publication files that were not recoverable as structured ZIP data are not represented as states.
| Captured | Edition | Application-product | Trade name | Strength | Dosage form / route | Product TE source text | RLD / RS | Approval date | Source SHA-256 |
|---|---|---|---|---|---|---|---|---|---|
| 2026-10-15 13:18:30 | 2026-09 | N050790-001 | RESTASIS | 0.05% | EMULSION / OPHTHALMIC | AB | RLD, RS | 2002-12-23 | c2088c7a36db… |
| 2026-10-15 13:18:30 | 2026-09 | N050790-002 | RESTASIS MULTIDOSE | 0.05% | EMULSION / OPHTHALMIC | RLD, RS | 2016-10-27 | c2088c7a36db… | |
| 2026-09-14 22:38:34 | 2026-08 | N050790-001 | RESTASIS | 0.05% | EMULSION / OPHTHALMIC | AB | RLD, RS | 2002-12-23 | 84e616aacf4f… |
| 2026-09-14 22:38:34 | 2026-08 | N050790-002 | RESTASIS MULTIDOSE | 0.05% | EMULSION / OPHTHALMIC | RLD, RS | 2016-10-27 | 84e616aacf4f… | |
| 2026-08-18 06:07:40 | 2026-07 | N050790-001 | RESTASIS | 0.05% | EMULSION / OPHTHALMIC | AB | RLD, RS | 2002-12-23 | caaa826d4ba7… |
| 2026-08-18 06:07:40 | 2026-07 | N050790-002 | RESTASIS MULTIDOSE | 0.05% | EMULSION / OPHTHALMIC | RLD, RS | 2016-10-27 | caaa826d4ba7… | |
| 2026-02-19 14:30 UTC | 2026-02 | N050790-001 | RESTASIS | 0.05% | EMULSION / OPHTHALMIC | AB | RLD, RS | 2002-12-23 | 011fe1cb6892… |
| 2026-02-19 14:30 UTC | 2026-02 | N050790-002 | RESTASIS MULTIDOSE | 0.05% | EMULSION / OPHTHALMIC | RLD, RS | 2016-10-27 | 011fe1cb6892… | |
| 2025-12-14 10:44 UTC · 2 captures of this ZIP | 2025-12 | N050790-001 | RESTASIS | 0.05% | EMULSION / OPHTHALMIC | AB | RLD, RS | 2002-12-23 | 31067a03dcf5… |
| 2025-12-14 10:44 UTC · 2 captures of this ZIP | 2025-12 | N050790-002 | RESTASIS MULTIDOSE | 0.05% | EMULSION / OPHTHALMIC | RLD, RS | 2016-10-27 | 31067a03dcf5… | |
| 2025-08-23 18:47 UTC | 2025-08 | N050790-001 | RESTASIS | 0.05% | EMULSION / OPHTHALMIC | AB | RLD, RS | 2002-12-23 | 6a471c1ec25d… |
| 2025-08-23 18:47 UTC | 2025-08 | N050790-002 | RESTASIS MULTIDOSE | 0.05% | EMULSION / OPHTHALMIC | RLD, RS | 2016-10-27 | 6a471c1ec25d… | |
| 2025-03-22 03:13 UTC · 3 captures of this ZIP | 2025-03 | N050790-001 | RESTASIS | 0.05% | EMULSION / OPHTHALMIC | AB | RLD, RS | 2002-12-23 | fd3edfee7708… |
| 2025-03-22 03:13 UTC · 3 captures of this ZIP | 2025-03 | N050790-002 | RESTASIS MULTIDOSE | 0.05% | EMULSION / OPHTHALMIC | RLD, RS | 2016-10-27 | fd3edfee7708… | |
| 2025-02-26 10:13 UTC · 3 captures of this ZIP | 2025-02 | N050790-001 | RESTASIS | 0.05% | EMULSION / OPHTHALMIC | AB | RLD, RS | 2002-12-23 | b8a1b40f171c… |
| 2025-02-26 10:13 UTC · 3 captures of this ZIP | 2025-02 | N050790-002 | RESTASIS MULTIDOSE | 0.05% | EMULSION / OPHTHALMIC | RLD, RS | 2016-10-27 | b8a1b40f171c… | |
| 2025-01-19 17:59 UTC · 7 captures of this ZIP | 2025-01 | N050790-001 | RESTASIS | 0.05% | EMULSION / OPHTHALMIC | AB | RLD, RS | 2002-12-23 | 03ed91905a0d… |
| 2025-01-19 17:59 UTC · 7 captures of this ZIP | 2025-01 | N050790-002 | RESTASIS MULTIDOSE | 0.05% | EMULSION / OPHTHALMIC | RLD, RS | 2016-10-27 | 03ed91905a0d… | |
| 2024-12-13 21:23 UTC · 2 captures of this ZIP | 2024-12 | N050790-001 | RESTASIS | 0.05% | EMULSION / OPHTHALMIC | AB | RLD, RS | 2002-12-23 | 2680178bc6a6… |
| 2024-12-13 21:23 UTC · 2 captures of this ZIP | 2024-12 | N050790-002 | RESTASIS MULTIDOSE | 0.05% | EMULSION / OPHTHALMIC | RLD, RS | 2016-10-27 | 2680178bc6a6… | |
| 2024-09-14 05:58 UTC · 2 captures of this ZIP | 2024-09 | N050790-001 | RESTASIS | 0.05% | EMULSION / OPHTHALMIC | AB | RLD, RS | 2002-12-23 | 5bbf6a4d5a75… |
| 2024-09-14 05:58 UTC · 2 captures of this ZIP | 2024-09 | N050790-002 | RESTASIS MULTIDOSE | 0.05% | EMULSION / OPHTHALMIC | RLD, RS | 2016-10-27 | 5bbf6a4d5a75… | |
| 2024-11-08 22:44 UTC · 3 captures of this ZIP | 2024-11 | N050790-001 | RESTASIS | 0.05% | EMULSION / OPHTHALMIC | AB | RLD, RS | 2002-12-23 | d8e5a09893c0… |
| 2024-11-08 22:44 UTC · 3 captures of this ZIP | 2024-11 | N050790-002 | RESTASIS MULTIDOSE | 0.05% | EMULSION / OPHTHALMIC | RLD, RS | 2016-10-27 | d8e5a09893c0… | |
| 2024-10-29 15:01 UTC | 2024-10 | N050790-001 | RESTASIS | 0.05% | EMULSION / OPHTHALMIC | AB | RLD, RS | 2002-12-23 | d06236e962d9… |
| 2024-10-29 15:01 UTC | 2024-10 | N050790-002 | RESTASIS MULTIDOSE | 0.05% | EMULSION / OPHTHALMIC | RLD, RS | 2016-10-27 | d06236e962d9… | |
| 2024-08-13 05:28 UTC · 3 captures of this ZIP | 2024-08 | N050790-001 | RESTASIS | 0.05% | EMULSION / OPHTHALMIC | AB | RLD, RS | 2002-12-23 | 79d66fd596c7… |
| 2024-08-13 05:28 UTC · 3 captures of this ZIP | 2024-08 | N050790-002 | RESTASIS MULTIDOSE | 0.05% | EMULSION / OPHTHALMIC | RLD, RS | 2016-10-27 | 79d66fd596c7… | |
| 2024-07-13 05:37 UTC · 2 captures of this ZIP | 2024-07 | N050790-001 | RESTASIS | 0.05% | EMULSION / OPHTHALMIC | AB | RLD, RS | 2002-12-23 | 301d65b070ca… |
| 2024-07-13 05:37 UTC · 2 captures of this ZIP | 2024-07 | N050790-002 | RESTASIS MULTIDOSE | 0.05% | EMULSION / OPHTHALMIC | RLD, RS | 2016-10-27 | 301d65b070ca… | |
| 2024-06-18 03:08 UTC · 5 captures of this ZIP | 2024-06 | N050790-001 | RESTASIS | 0.05% | EMULSION / OPHTHALMIC | AB | RLD, RS | 2002-12-23 | 1e350fbaab3a… |
| 2024-06-18 03:08 UTC · 5 captures of this ZIP | 2024-06 | N050790-002 | RESTASIS MULTIDOSE | 0.05% | EMULSION / OPHTHALMIC | RLD, RS | 2016-10-27 | 1e350fbaab3a… | |
| 2024-05-31 18:47 UTC | 2024-05 | N050790-001 | RESTASIS | 0.05% | EMULSION / OPHTHALMIC | AB | RLD, RS | 2002-12-23 | 8072bd15b7f6… |
| 2024-05-31 18:47 UTC | 2024-05 | N050790-002 | RESTASIS MULTIDOSE | 0.05% | EMULSION / OPHTHALMIC | RLD, RS | 2016-10-27 | 8072bd15b7f6… | |
| 2022-06-29 02:47 UTC · 2 captures of this ZIP | 2022-06 | N050790-001 | RESTASIS | 0.05% | EMULSION / OPHTHALMIC | AB | RLD, RS | 2002-12-23 | 5c6f7cd8ea54… |
| 2022-06-29 02:47 UTC · 2 captures of this ZIP | 2022-06 | N050790-002 | RESTASIS MULTIDOSE | 0.05% | EMULSION / OPHTHALMIC | RLD, RS | 2016-10-27 | 5c6f7cd8ea54… | |
| 2022-04-08 23:34 UTC | 2022-04 | N050790-001 | RESTASIS | 0.05% | EMULSION / OPHTHALMIC | AB | RLD, RS | 2002-12-23 | 5d02ea3f76ae… |
| 2022-04-08 23:34 UTC | 2022-04 | N050790-002 | RESTASIS MULTIDOSE | 0.05% | EMULSION / OPHTHALMIC | RLD, RS | 2016-10-27 | 5d02ea3f76ae… | |
| 2022-04-04 05:41 UTC | 2022-04 | N050790-001 | RESTASIS | 0.05% | EMULSION / OPHTHALMIC | AB | RLD, RS | 2002-12-23 | 4b0b4de00fa7… |
| 2022-04-04 05:41 UTC | 2022-04 | N050790-002 | RESTASIS MULTIDOSE | 0.05% | EMULSION / OPHTHALMIC | RLD, RS | 2016-10-27 | 4b0b4de00fa7… |
| Captured | Edition | Application-product | TE code | Order | Source SHA-256 |
|---|---|---|---|---|---|
| 2026-10-15 13:18:30 | 2026-09 | N050790-001 | AB | 1 | c2088c7a36db… |
| 2026-09-14 22:38:34 | 2026-08 | N050790-001 | AB | 1 | 84e616aacf4f… |
| 2026-08-18 06:07:40 | 2026-07 | N050790-001 | AB | 1 | caaa826d4ba7… |
| 2026-02-19 14:30 UTC | 2026-02 | N050790-001 | AB | 1 | 011fe1cb6892… |
| 2025-12-14 10:44 UTC · 2 captures of this ZIP | 2025-12 | N050790-001 | AB | 1 | 31067a03dcf5… |
| 2025-08-23 18:47 UTC | 2025-08 | N050790-001 | AB | 1 | 6a471c1ec25d… |
| 2025-03-22 03:13 UTC · 3 captures of this ZIP | 2025-03 | N050790-001 | AB | 1 | fd3edfee7708… |
| 2025-02-26 10:13 UTC · 3 captures of this ZIP | 2025-02 | N050790-001 | AB | 1 | b8a1b40f171c… |
| 2025-01-19 17:59 UTC · 7 captures of this ZIP | 2025-01 | N050790-001 | AB | 1 | 03ed91905a0d… |
| 2024-12-13 21:23 UTC · 2 captures of this ZIP | 2024-12 | N050790-001 | AB | 1 | 2680178bc6a6… |
| 2024-09-14 05:58 UTC · 2 captures of this ZIP | 2024-09 | N050790-001 | AB | 1 | 5bbf6a4d5a75… |
| 2024-11-08 22:44 UTC · 3 captures of this ZIP | 2024-11 | N050790-001 | AB | 1 | d8e5a09893c0… |
| 2024-10-29 15:01 UTC | 2024-10 | N050790-001 | AB | 1 | d06236e962d9… |
| 2024-08-13 05:28 UTC · 3 captures of this ZIP | 2024-08 | N050790-001 | AB | 1 | 79d66fd596c7… |
| 2024-07-13 05:37 UTC · 2 captures of this ZIP | 2024-07 | N050790-001 | AB | 1 | 301d65b070ca… |
| 2024-06-18 03:08 UTC · 5 captures of this ZIP | 2024-06 | N050790-001 | AB | 1 | 1e350fbaab3a… |
| 2024-05-31 18:47 UTC | 2024-05 | N050790-001 | AB | 1 | 8072bd15b7f6… |
| 2022-06-29 02:47 UTC · 2 captures of this ZIP | 2022-06 | N050790-001 | AB | 1 | 5c6f7cd8ea54… |
| 2022-04-08 23:34 UTC | 2022-04 | N050790-001 | AB | 1 | 5d02ea3f76ae… |
| 2022-04-04 05:41 UTC | 2022-04 | N050790-001 | AB | 1 | 4b0b4de00fa7… |
| 2022-03-09 01:35 UTC | 2022-03 | N050790-001 | AB | 1 | bb7c543d1eb4… |
| 2024-03-16 18:09 UTC · 4 captures of this ZIP | 2024-03 | N050790-001 | AB | 1 | 6a51e52b5d6a… |
| 2024-02-18 07:12 UTC | 2024-02 | N050790-001 | AB | 1 | 1c564ffb4f44… |
| 2023-12-20 04:57 UTC | 2023-12 | N050790-001 | AB | 1 | ea1830bbd6c7… |
| 2023-11-28 05:40 UTC · 2 captures of this ZIP | 2023-11 | N050790-001 | AB | 1 | a72a2bbeb626… |
| 2023-10-25 00:34 UTC · 2 captures of this ZIP | 2023-10 | N050790-001 | AB | 1 | 9b2671bbb829… |
| 2023-07-15 15:27 UTC · 2 captures of this ZIP | 2023-07 | N050790-001 | AB | 1 | a67488948f0b… |
| 2023-06-13 01:57 UTC · 3 captures of this ZIP | 2023-06 | N050790-001 | AB | 1 | 3f0d92c62455… |
| 2023-05-13 08:27 UTC | 2023-05 | N050790-001 | AB | 1 | 053a50430f4f… |
| 2023-01-26 05:58 UTC | 2023-01 | N050790-001 | AB | 1 | 3bdfa0b2c4d7… |
| 2022-11-12 20:34 UTC · 5 captures of this ZIP | 2022-11 | N050790-001 | AB | 1 | 3a93d1ddd44b… |
| 2022-10-28 04:53 UTC | 2022-10 | N050790-001 | AB | 1 | f41ea6bd6efb… |
| 2022-09-29 23:25 UTC | 2022-09 | N050790-001 | AB | 1 | e64feba35796… |
| 2022-07-09 03:26 UTC · 3 captures of this ZIP | 2022-07 | N050790-001 | AB | 1 | cb3db0bc1861… |
| 2026-07-26 02:55 UTC · 3 captures of this ZIP | 2026-06 | N050790-001 | AB | 1 | a50c72e98297… |
| Captured | Edition | Application-product | Patent | Expiration | Use code | Coverage / status | Submission date | Source SHA-256 |
|---|---|---|---|---|---|---|---|---|
| 2026-10-15 13:18:30 | 2026-09 | N050790-002 | 8292129 | 2031-02-25 | Drug product, Delist requested | 2017-06-26 | c2088c7a36db… | |
| 2026-10-15 13:18:30 | 2026-09 | N050790-002 | 8561859 | 2032-04-16 | Drug product, Delist requested | 2017-06-26 | c2088c7a36db… | |
| 2026-10-15 13:18:30 | 2026-09 | N050790-002 | 9676525 | 2034-02-07 | Drug product, Delist requested | 2017-06-26 | c2088c7a36db… | |
| 2026-10-15 13:18:30 | 2026-09 | N050790-002 | 9669974 | 2034-05-11 | Drug product, Delist requested | 2017-06-26 | c2088c7a36db… | |
| 2026-09-14 22:38:34 | 2026-08 | N050790-002 | 8292129 | 2031-02-25 | Drug product, Delist requested | 2017-06-26 | 84e616aacf4f… | |
| 2026-09-14 22:38:34 | 2026-08 | N050790-002 | 8561859 | 2032-04-16 | Drug product, Delist requested | 2017-06-26 | 84e616aacf4f… | |
| 2026-09-14 22:38:34 | 2026-08 | N050790-002 | 9676525 | 2034-02-07 | Drug product, Delist requested | 2017-06-26 | 84e616aacf4f… | |
| 2026-09-14 22:38:34 | 2026-08 | N050790-002 | 9669974 | 2034-05-11 | Drug product, Delist requested | 2017-06-26 | 84e616aacf4f… | |
| 2026-08-18 06:07:40 | 2026-07 | N050790-002 | 8292129 | 2031-02-25 | Drug product, Delist requested | 2017-06-26 | caaa826d4ba7… | |
| 2026-08-18 06:07:40 | 2026-07 | N050790-002 | 8561859 | 2032-04-16 | Drug product, Delist requested | 2017-06-26 | caaa826d4ba7… | |
| 2026-08-18 06:07:40 | 2026-07 | N050790-002 | 9676525 | 2034-02-07 | Drug product, Delist requested | 2017-06-26 | caaa826d4ba7… | |
| 2026-08-18 06:07:40 | 2026-07 | N050790-002 | 9669974 | 2034-05-11 | Drug product, Delist requested | 2017-06-26 | caaa826d4ba7… | |
| 2026-02-19 14:30 UTC | 2026-02 | N050790-002 | 8292129 | 2031-02-25 | Drug product, Delist requested | 2017-06-26 | 011fe1cb6892… | |
| 2026-02-19 14:30 UTC | 2026-02 | N050790-002 | 8561859 | 2032-04-16 | Drug product, Delist requested | 2017-06-26 | 011fe1cb6892… | |
| 2026-02-19 14:30 UTC | 2026-02 | N050790-002 | 9676525 | 2034-02-07 | Drug product, Delist requested | 2017-06-26 | 011fe1cb6892… | |
| 2026-02-19 14:30 UTC | 2026-02 | N050790-002 | 9669974 | 2034-05-11 | Drug product, Delist requested | 2017-06-26 | 011fe1cb6892… | |
| 2025-12-14 10:44 UTC · 2 captures of this ZIP | 2025-12 | N050790-002 | 8292129 | 2031-02-25 | Drug product, Delist requested | 2017-06-26 | 31067a03dcf5… | |
| 2025-12-14 10:44 UTC · 2 captures of this ZIP | 2025-12 | N050790-002 | 8561859 | 2032-04-16 | Drug product, Delist requested | 2017-06-26 | 31067a03dcf5… | |
| 2025-12-14 10:44 UTC · 2 captures of this ZIP | 2025-12 | N050790-002 | 9676525 | 2034-02-07 | Drug product, Delist requested | 2017-06-26 | 31067a03dcf5… | |
| 2025-12-14 10:44 UTC · 2 captures of this ZIP | 2025-12 | N050790-002 | 9669974 | 2034-05-11 | Drug product, Delist requested | 2017-06-26 | 31067a03dcf5… | |
| 2025-08-23 18:47 UTC | 2025-08 | N050790-002 | 8292129 | 2031-02-25 | Drug product, Delist requested | 2017-06-26 | 6a471c1ec25d… | |
| 2025-08-23 18:47 UTC | 2025-08 | N050790-002 | 8561859 | 2032-04-16 | Drug product, Delist requested | 2017-06-26 | 6a471c1ec25d… | |
| 2025-08-23 18:47 UTC | 2025-08 | N050790-002 | 9676525 | 2034-02-07 | Drug product, Delist requested | 2017-06-26 | 6a471c1ec25d… | |
| 2025-08-23 18:47 UTC | 2025-08 | N050790-002 | 9669974 | 2034-05-11 | Drug product, Delist requested | 2017-06-26 | 6a471c1ec25d… | |
| 2025-03-22 03:13 UTC · 3 captures of this ZIP | 2025-03 | N050790-002 | 8292129 | 2031-02-25 | Drug product | 2017-06-26 | fd3edfee7708… | |
| 2025-03-22 03:13 UTC · 3 captures of this ZIP | 2025-03 | N050790-002 | 8561859 | 2032-04-16 | Drug product | 2017-06-26 | fd3edfee7708… | |
| 2025-03-22 03:13 UTC · 3 captures of this ZIP | 2025-03 | N050790-002 | 9676525 | 2034-02-07 | Drug product | 2017-06-26 | fd3edfee7708… | |
| 2025-03-22 03:13 UTC · 3 captures of this ZIP | 2025-03 | N050790-002 | 9669974 | 2034-05-11 | Drug product | 2017-06-26 | fd3edfee7708… | |
| 2025-02-26 10:13 UTC · 3 captures of this ZIP | 2025-02 | N050790-002 | 8292129 | 2031-02-25 | Drug product | 2017-06-26 | b8a1b40f171c… | |
| 2025-02-26 10:13 UTC · 3 captures of this ZIP | 2025-02 | N050790-002 | 8561859 | 2032-04-16 | Drug product | 2017-06-26 | b8a1b40f171c… | |
| 2025-02-26 10:13 UTC · 3 captures of this ZIP | 2025-02 | N050790-002 | 9676525 | 2034-02-07 | Drug product | 2017-06-26 | b8a1b40f171c… | |
| 2025-02-26 10:13 UTC · 3 captures of this ZIP | 2025-02 | N050790-002 | 9669974 | 2034-05-11 | Drug product | 2017-06-26 | b8a1b40f171c… | |
| 2025-01-19 17:59 UTC · 7 captures of this ZIP | 2025-01 | N050790-002 | 8629111 | 2024-08-27 | Drug product, Delist requested | 2016-11-18 | 03ed91905a0d… | |
| 2025-01-19 17:59 UTC · 7 captures of this ZIP | 2025-01 | N050790-002 | 8633162 | 2024-08-27 | U-1479 | Delist requested | 2016-11-18 | 03ed91905a0d… |
| 2025-01-19 17:59 UTC · 7 captures of this ZIP | 2025-01 | N050790-002 | 8642556 | 2024-08-27 | Drug product, Delist requested | 2016-11-18 | 03ed91905a0d… | |
| 2025-01-19 17:59 UTC · 7 captures of this ZIP | 2025-01 | N050790-002 | 8648048 | 2024-08-27 | U-1483 | Delist requested | 2016-11-18 | 03ed91905a0d… |
| 2025-01-19 17:59 UTC · 7 captures of this ZIP | 2025-01 | N050790-002 | 8685930 | 2024-08-27 | Drug product, Delist requested | 2016-11-18 | 03ed91905a0d… | |
| 2025-01-19 17:59 UTC · 7 captures of this ZIP | 2025-01 | N050790-002 | 9248191 | 2024-08-27 | U-1479 | Delist requested | 2016-11-18 | 03ed91905a0d… |
| 2025-01-19 17:59 UTC · 7 captures of this ZIP | 2025-01 | N050790-002 | 8292129 | 2031-02-25 | Drug product | 2017-06-26 | 03ed91905a0d… | |
| 2025-01-19 17:59 UTC · 7 captures of this ZIP | 2025-01 | N050790-002 | 8561859 | 2032-04-16 | Drug product | 2017-06-26 | 03ed91905a0d… |
OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.
| Brand | Generic | Manufacturer | SPL set ID | Effective date | Available safety fields | Join |
|---|---|---|---|---|---|---|
| RESTASIS | CYCLOSPORINE | Allergan, Inc. | 8e24af2b-bc1c-4849-94f2-6df950cdca89 | 2024-09-09 | Warnings, Adverse reactions | 0023-9163 |
| 10aaf531-4033-442c-821d-69292ccf5f85 | 8227ca35-77c1-4a08-87a3-7dcefef39bc5 | 2010-05-27 | Warnings, Adverse reactions | 10aaf531-4033-442c-821d-69292ccf5f85 8227ca35-77c1-4a08-87a3-7dcefef39bc5 |
Adverse event summaries are temporarily unavailable. Other product information remains available.