NDC 68071-4859-01 - diclofenac sodium
This NDC is not currently matched to an FDA NDC product listing in FDA.report, but it is a valid NDC-form code. FDA.report is showing the available DailyMed label context for the product root.
- Product NDC
- 68071-4859
- Requested NDC
- 68071-4859-01
- Package NDCs from labels
- 68071-4859-1, 68071-4859-01
- Manufacturer
- NuCare Pharmaceuticals,Inc.
- Effective date
- 2024-06-14
- Current FDA listing
- Not matched in FDA.report NDC product tables
DailyMed Labels#
| Label | Manufacturer | Effective date | Type |
|---|---|---|---|
| Diclofenac Sodium Gel, 3% | NuCare Pharmaceuticals,Inc. | 2024-06-14 | HUMAN PRESCRIPTION DRUG LABEL |
FDA-Initiated Inactive NDC Indexing#
| NDC | Effective | Action | Document | Indexing SPL | Related label |
|---|---|---|---|---|---|
| 68071-4859-1 | 2021-02-17 | C162847 | 48780-1 | ba0f9c33-11c4-a910-e053-dadaa90a0b85 | Diclofenac Sodium Gel, 3% |
| 68071-4859-1 | 2021-01-29 | C162847 | 48780-1 | ba0f9c33-11c4-a910-e053-dadaa90a0b85 | Diclofenac Sodium Gel, 3% |
DailyMed Package Descriptions#
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 68071-4859-1 | diclofenac sodium | 100 g in 1 BOX | GEL | 100 | 4 |
DailyMed Dashboard NDC Coverage#
| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|---|---|---|---|
| 68071-4859 | DICLOFENAC SODIUM GEL [NUCARE PHARMACEUTICALS,INC.] | 4 | Current NDC, Legacy NDC, 1 package rows | 20240616_8721da56-0f8a-5903-e053-2991aa0a61b5.zip |
openFDA label cross-check#
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 |
|---|---|---|---|---|---|---|
| Diclofenac Sodium Delayed Release | DICLOFENAC SODIUM | REMEDYREPACK INC. | ddd2278b-70be-41ca-8a84-e3fe0f1a1561 | 2026-07-28 | Boxed warning, Warnings, Adverse reactions | QTG126297Q |
| Lidocaine Plus Pain Relieving | LIDOCAINE HYDROCHLORIDE, BENZYL ALCOHOL | CVS Pharmacy | 49003aac-184c-ae33-e063-6294a90a29c0 | 2026-07-24 | Warnings | LKG8494WBH |
| Diclofenac sodium | DICLOFENAC SODIUM | CVS Pharmacy | 591cc2ed-e667-4779-a426-8a2e6f873573 | 2026-07-22 | Warnings | QTG126297Q |
| Sterile Water | WATER | Cardinal Health 107, LLC | 9655cd02-82b5-4a75-813b-854b19551481 | 2026-07-21 | Warnings, Adverse reactions | 059QF0KO0R |
| DICLOFENAC SODIUM | DICLOFENAC SODIUM | Aurobindo Pharma Limited | d9b6f1d0-1710-46fb-8ea4-80b3ca60a575 | 2026-07-17 | Boxed warning, Warnings, Adverse reactions | QTG126297Q |
| DICLOFENAC SODIUM | DICLOFENAC SODIUM | HAWAII REPACK, INC | ea113a58-c7ed-4768-9777-93d9b166dfbe | 2026-07-12 | Boxed warning, Warnings, Adverse reactions | 855642 QTG126297Q |
| Diclofenac Sodium | DICLOFENAC SODIUM 1% | Sportpharm LLC | 391d9d0b-74b7-4359-aea0-d3bb8c8d3cd1 | 2026-07-10 | Warnings | QTG126297Q |
| Diclofenac Sodium | DICLOFENAC SODIUM | American Health Packaging | 63c00b50-06d3-4659-81cf-be4516429e81 | 2026-07-10 | Boxed warning, Warnings, Adverse reactions | QTG126297Q |
| DICLOFENAC SODIUM | DICLOFENAC SODIUM | REMEDYREPACK INC. | 6e6a6f98-5517-4f67-9a6a-71019ba2d773 | 2026-07-09 | Boxed warning, Warnings, Adverse reactions | QTG126297Q |
| Diclofenac sodium | DICLOFENAC SODIUM | Preferred Pharmaceuticals Inc. | 71a823c4-9c88-474d-b525-276f9e7808aa | 2026-07-07 | Boxed warning, Warnings, Adverse reactions | 855642 QTG126297Q |
| Dr. Drop NMN Vital Balance (Drop No.1 Cream 90g) | NMN (NICOTINAMIDE MONONUCLEOTIDE), ECTOIN (ECTOINE) | Reedfresh Co., LTD | 55d703ca-ff9d-0dbc-e063-6294a90ab6b1 | 2026-07-05 | Warnings | 059QF0KO0R |
| Diclofenac Sodium | DICLOFENAC SODIUM | Preferred Pharmaceuticals Inc. | 09643e65-f301-4891-96f4-d78bf3621e23 | 2026-07-02 | Warnings | QTG126297Q |
| Diclofenac Sodium Delayed Release | DICLOFENAC SODIUM | REMEDYREPACK INC. | 30c7e4fd-30af-4d28-a6ef-7386ff83cfb8 | 2026-07-02 | Boxed warning, Warnings, Adverse reactions | QTG126297Q |
| Eyesaline Eyewash Concentrate | PURIFIED WATER | Protective Industrial Products, Inc. | 558e5926-9027-d3f6-e063-6294a90ab121 | 2026-07-02 | Warnings | 059QF0KO0R |
| Fendall 2000 Pure Flow | PURIFIED WATER | Protective Industrial Products, Inc. | 55a1d07e-0006-0c75-e063-6394a90a7acc | 2026-07-02 | Warnings | 059QF0KO0R |
| Fendall 1000 Pure Flow | PURIFIED WATER | Protective Industrial Products, Inc. | 55a2f4da-bb1e-8ead-e063-6394a90af72e | 2026-07-02 | Warnings | 059QF0KO0R |
| Sterile Eyesaline Eyewash | STERILE EYESALINE EYEWASH | Protective Industrial Products, Inc. | 55a290e8-8310-8be4-e063-6394a90abdce | 2026-07-02 | Warnings | 059QF0KO0R |
| Eyesaline Emergency Eyewash | PURIFIED WATER | Protective Industrial Products, Inc. | 55a261c2-725d-6765-e063-6294a90a3260 | 2026-07-02 | Warnings | 059QF0KO0R |
| Remodulin | TREPROSTINIL | United Therapeutics Corporation | 6c80bb38-e8db-4138-9f0d-dbbf9c673185 | 2026-07-02 | Warnings, Adverse reactions | 059QF0KO0R |
| Diclofenac Sodium | DICLOFENAC SODIUM | American Health Packaging | dbb1489d-b690-4e53-905d-7fb07ad263b3 | 2026-07-01 | Boxed warning, Warnings, Adverse reactions | QTG126297Q |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.