Oxybutynin Chloride Tablets, USP

Manufacturer
State of Florida DOH Central Pharmacy
Effective date
2010-06-07
Label type
HUMAN PRESCRIPTION DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-05-31 20:08:43

Label at a glance#

ProductOxybutynin Chloride
Active ingredientOXYBUTYNIN CHLORIDE
Label structure11 sections

Indications and uses

Oxybutynin chloride tablets are indicated for the relief of symptoms of bladder instability associated with voiding in patients with uninhibited neurogenic or reflex neurogenic bladder (i.e., urgency, frequency, urinary leakage, urge incontinence, dysuria).

Dosage and administration

Adults: The usual dose is one 5 mg tablet two to three times a day. The maximum recommended dose is one tablet (5 mg) four times a day. Children over 5 years of age: The usual dose is one 5 mg tablet two times a day. The maximum recommended dose is one tablet (5 mg) three times a day.

Label contents#

Full prescribing information#

DESCRIPTION

DESCRIPTION SECTION

Oxybutynin chloride is a white crystalline solid, readily soluble in water and acids, but relatively insoluble in alkalis. Chemically, it is the d,i-(racemic) form of 4-diethyl-amino-2-butynyl phenylcyclohexylglycolate hydrochloride with the following formula:

C22H32ClNO3 Structural FormulaStructural Formula M.W. 393.9

Each tablet for oral administration contains oxybutynin chloride, USP 5 mg.

Inactive ingredients include calcium stearate, microcrystalline cellulose, anhydrous lactose, sodium starch glycolate and FD&C Blue #1.

CLINICAL PHARMACOLOGY

CLINICAL PHARMACOLOGY SECTION

Oxybutynin chloride exerts direct antispasmodic effect on smooth muscle and inhibits the muscarinic action of acetylcholine on smooth muscle. It exhibits only one-fifth of the anticholinergic activity of atropine on the rabbit detrusor muscle, but four to ten times the antispasmodic activity. No blocking effects occur at skeletal neuromuscular junctions or autonomic ganglia (antinicotinic effects).

Oxybutynin relaxes bladder smooth muscle. In patients with conditions characterized by involuntary bladder contractions, cystometric studies have demonstrated that oxybutynin increases bladder (vesical) capacity, diminishes the frequency of uninhibited contractions of the detrusor muscle, and delays the initial desire to void. Oxybutynin thus decreases urgency and the frequency of both incontinent episodes and voluntary urination.

Oxybutynin chloride was well tolerated in patients administered the drug in controlled studies of 30 days duration and in uncontrolled studies in which some of the patients received the drug for two years. Pharmacokinetic information is not currently available.

INDICATIONS AND USAGE

INDICATIONS & USAGE SECTION

Oxybutynin chloride tablets are indicated for the relief of symptoms of bladder instability associated with voiding in patients with uninhibited neurogenic or reflex neurogenic bladder (i.e., urgency, frequency, urinary leakage, urge incontinence, dysuria).

CONTRAINDICATIONS

CONTRAINDICATIONS SECTION

Oxybutynin chloride is contraindicated in patients with untreated angle closure glaucoma and in patients with untreated narrow anterior chamber angles since anticholinergic drugs may aggravate these conditions. It is also contraindicated in partial or complete obstruction of the gastrointestinal tract, paralytic ileus, intestinal atony of the elderly or debilitated patient, megacolon, toxic megacolon complicating ulcerative colitis, severe colitis and myasthenia gravis. It is contraindicated in patients with obstructive uropathy and in patients with unstable cardiovascular status in acute hemorrhage.

Oxybutynin chloride is contraindicated in patients who have demonstrated hypersensitivity to the product.

WARNINGS

WARNINGS SECTION

Oxybutynin chloride, when administered in the presence of high environmental temperature, can cause heat prostration (fever and heat stroke due to decreased sweating). Diarrhea may be an early symptom of incomplete intestinal obstruction, especially in patients with ileostomy or colostomy. In this instance, treatment with oxybutynin chloride would be inappropriate and possibly harmful.

Oxybutynin chloride may produce drowsiness or blurred vision. The patient should be cautioned regarding activities requiring mental alertness such as operating a motor vehicle or other machinery or performing hazardous work while taking this drug.

Alcohol or other sedative drugs may enhance the drowsiness caused by oxybutynin.

PRECAUTIONS

PRECAUTIONS SECTION

Oxybutynin chloride should be used with caution in the elderly and in all patients with autonomic neuropathy, hepatic or renal disease. Oxybutynin may aggravate the symptoms of hyperthyroidism, coronary heart disease, congestive heart failure, cardiac arrhythmias, hiatal hernia, tachycardia, hypertension, and prostatic hypertrophy.

Administration of oxybutynin chloride to patients with ulcerative colitis may suppress intestinal motility to the point of producing a paralytic ileus and precipitate or aggravate toxic megacolon, a serious complication of the disease.

Carcinogenesis, Mutagenesis, Impairment of Fertility

CARCINOGENESIS & MUTAGENESIS & IMPAIRMENT OF FERTILITY SECTION

A 24-month study in rats at dosages up to approximately 400 times the recommended human dosage showed no evidence of carcinogenicity.

Oxybutynin showed no increase in mutagenic activity when tested in Schizosac-charomyces pompholiciformis, Saccharomyces cerevisiae, and Salmonella typhimurium test symptoms. Reproduction studies in the hamster, rabbit, rat, and mouse have shown no definite evidence of impaired fertility.

Pregnancy

PREGNANCY SECTION

Category B: Reproduction studies in the hamster, rabbit, rat, and mouse have shown no definite evidence of impaired fertility or harm to the animal fetus. The safety of oxybutynin chloride administered to women who are or who may become pregnant has not been established. Therefore, oxybutynin should not be given to pregnant women unless, in the judgment of the physician, the probable clinical benefits outweigh the possible hazards.

Nursing Mothers

NURSING MOTHERS SECTION

It is not known whether this drug is excreted in human milk. Because many drugs are excreted in human milk, caution should be exercised when oxybutynin chloride is administered to a nursing woman.

Pediatric Use

PEDIATRIC USE SECTION

The safety and efficacy of oxybutynin chloride administration have been demonstrated for children 5 years of age and older (see DOSAGE AND ADMINISTRATION). However, as there is insufficient clinical data for children under age 5, oxybutynin is not recommended for this age group.

ADVERSE REACTIONS

ADVERSE REACTIONS SECTION

Following administration of oxybutynin chloride, the symptoms that can be associated with the use of other anticholinergic drugs may occur:

Cardiovascular: Palpitations, tachycardia, vasodilatation.

Dermatologic: Decreased sweating, rash.

Gastrointestinal/Genitourinary: Constipation, decreased gastrointestinal motility, dry mouth, nausea, urinary hesitance and retention.

Nervous System: Asthenia, dizziness, drowsiness, hallucinations, insomnia, restlessness.

Ophthalmic: Amblyopia, cycloplegia, decreased lacrimation, mydriasis.

Other: Impotence, suppression of lactation.

OVERDOSAGE

OVERDOSAGE SECTION

The symptoms of overdosage with oxybutynin chloride may be any of those seen with other anticholinergic agents. Symptoms may include signs of central nervous system excitation (e.g., restlessness, tremor, irritability, convulsions, delirium, hallucinations), flushing, fever, nausea, vomiting, tachycardia, hypotension or hypertension, respiratory failure, paralysis, or coma.

In the event of an overdose or exaggerated response, treatment should be symptomatic and supportive. Maintain respiration and induce emesis or perform gastric lavage (emesis is contraindicated in precomatose, convulsive, or psychotic state). Activated charcoal may be administered as well as a cathartic. Physostigmine may be considered to reverse symptoms of anticholinergic intoxication.

Hyperpyrexia may be treated symptomatically with ice bags or other cold applications and alcohol sponges.

DOSAGE AND ADMINISTRATION

DOSAGE & ADMINISTRATION SECTION

Adults: The usual dose is one 5 mg tablet two to three times a day. The maximum recommended dose is one tablet (5 mg) four times a day.

Children over 5 years of age: The usual dose is one 5 mg tablet two times a day. The maximum recommended dose is one tablet (5 mg) three times a day.

HOW SUPPLIED

HOW SUPPLIED SECTION

Oxybutynin Chloride Tablets, USP:

5 mg — Very pale blue, round, scored tablets.

Debossed: PLIVA 456

They are supplied by State of Florida DOH Central Pharmacy as follows:

NDCStrengthQuantity/FormColorSource Prod. Code
53808-0747-15 mg30 Tablets in a Blister PackVery pale blue50111-456

Dispense in a tight, light-resistant container as defined in the USP.

Store at 20°-25°C (68°-77°F) [See USP Controlled Room Temperature].

Manufactured by:

PLIVA®, Inc.

East Hanover, NJ  07936

This Product was Repackaged By:

State of Florida DOH Central Pharmacy
104-2 Hamilton Park Drive
Tallahassee, FL 32304
United States

Label Image 5mg

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Label Image for 5mg
Label Image for 5mg

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
863664oxyBUTYnin chloride 5 MG Oral TabletPSN1
863664oxybutynin chloride 5 MG Oral TabletSCD1

DailyMed Pharmacologic Classes#

Class, Version, Type table
ClassVersionTypeEffective
OXYBUTYNIN Pharmacologic Class Indexing2Indexing - Pharmacologic Class20180813

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
3544f362-07fc-93b1-457b-1fba00be087aProduct name820230316
4daffbf2-44c8-ca46-d284-5db69e1e6ef4Product name820210525
982338c6-c45c-b6b4-1452-14b01fbdf98dProduct name220180801
054197ba-7ed3-0ddb-321e-dbb51c0fe9b6Product name220171212
3544f362-07fc-93b1-457b-1fba00be087aProduct name220171212
8b00ae7e-01f2-f83c-632e-edfc23808364Product name120140508

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
53808-0747-12020-01-31C16284748780-19d75b9d0-efe0-f424-e053-dadaa90a57ceOxybutynin Chloride Tablets, USP

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
53808-0747-1Oxybutynin Chloride30 in 1 BLISTER PACKTABLET301

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
53808-0747OXYBUTYNIN CHLORIDE TABLET [STATE OF FLORIDA DOH CENTRAL PHARMACY]1Legacy NDC, 1 package rows20100611_d2aa1b90-bea7-4a93-b2e7-22710548ff55.zip

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDCBilling unitProduct NDCDailyMed indexing SPLSPL versionEffective
50111-456-01EA - Each50111-4564c8ca356-7fd1-4818-8ac7-906b87bca92d12012-07-24
50111-456-02EA - Each50111-4566f3c41c8-421e-4e28-94a8-3cbce353632c12012-07-24
50111-456-03EA - Each50111-4569b6b2ff6-8b9d-4078-ab17-cab3d192975d12012-07-24

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
IngredientTypeUNIISPL versionUploaded
OXYBUTYNIN CHLORIDEACTIVE INGREDIENTL9F3D9RENQ1
OXYBUTYNINACTIVE MOIETYK9P6MC70921
ANHYDROUS LACTOSEINACTIVE INGREDIENT3SY5LH9PMK1
CALCIUM STEARATEINACTIVE INGREDIENT776XM7047L1
CELLULOSE, MICROCRYSTALLINEINACTIVE INGREDIENTOP1R32D61U1
FD&C BLUE NO. 1INACTIVE INGREDIENTH3R47K3TBD1
SODIUM STARCH GLYCOLATE TYPE A POTATOINACTIVE INGREDIENT5856J3G2A21

Products#

Every source-derived product name is available through these pages.

DailyMed product names page 1 of 1 · 7 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
53808-074753808-0747-1
50111-456

Ingredients#

Every source-derived ingredient row is available through these pages.

DailyMed ingredient rows page 1 of 1 · 6 matching rows.

Source Document#

Source XML

Inactive ingredient matches#

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.

Inactive ingredient links page 1 of 1 · 4 matching rows.

DailyMed ingredient, IID ingredient, UNII table
DailyMed ingredientIID ingredientUNIIDosage form / routePotencyMaximum daily exposureMatch
CALCIUM STEARATECALCIUM STEARATE776XM7047LTABLET / ORAL280 mgExact identifier — unii+route+dosage form
CELLULOSE, MICROCRYSTALLINEMICROCRYSTALLINE CELLULOSEOP1R32D61UTABLET / ORAL6184 mgExact identifier — unii+route+dosage form
FD&C BLUE NO. 1FD&C BLUE NO. 1H3R47K3TBDTABLET / ORAL27.53 mgExact identifier — unii+route+dosage form
ANHYDROUS LACTOSEANHYDROUS LACTOSE3SY5LH9PMKTABLET / ORAL6795 mgExact identifier — unii+route+dosage form

Orange Book application contexts#

All distinct exact application/product contexts derived from this label’s complete NDC list are paginated below.

Orange Book application contexts page 1 of 1 · 1 matching rows.

Source provenance: Browse the complete Orange Book source catalog · source snapshot 43.

Orange Book products#

Current product rows page 1 of 1 · 1 matching rows.

Application-product, Trade name, Ingredient table
Application-productTrade nameIngredientStrengthDosage form / routeTE codesRLD / RSApproval date
A071655-001OXYBUTYNIN CHLORIDEOXYBUTYNIN CHLORIDE5MGTABLET / ORALAB1988-11-14

Therapeutic equivalence codes#

Current TE-code rows page 1 of 1 · 1 matching rows.

Application-product, TE code table
Application-productTE code
A071655-001AB

Observed Orange Book product history#

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.

Product history page 1 of 2 · 43 observed states.

Captured, Edition, Application-product table
CapturedEditionApplication-productTrade nameStrengthDosage form / routeProduct TE source textRLD / RSApproval dateSource SHA-256
2026-09-14 22:38:342026-08A071655-001OXYBUTYNIN CHLORIDE5MGTABLET / ORALAB1988-11-1484e616aacf4f…
2026-08-18 06:07:402026-07A071655-001OXYBUTYNIN CHLORIDE5MGTABLET / ORALAB1988-11-14caaa826d4ba7…
2026-02-19 14:30 UTC2026-02A071655-001OXYBUTYNIN CHLORIDE5MGTABLET / ORALAB1988-11-14011fe1cb6892…
2025-12-14 10:44 UTC · 2 captures of this ZIP2025-12A071655-001OXYBUTYNIN CHLORIDE5MGTABLET / ORALAB1988-11-1431067a03dcf5…
2025-08-23 18:47 UTC2025-08A071655-001OXYBUTYNIN CHLORIDE5MGTABLET / ORALAB1988-11-146a471c1ec25d…
2025-03-22 03:13 UTC · 3 captures of this ZIP2025-03A071655-001OXYBUTYNIN CHLORIDE5MGTABLET / ORALAB1988-11-14fd3edfee7708…
2025-02-26 10:13 UTC · 3 captures of this ZIP2025-02A071655-001OXYBUTYNIN CHLORIDE5MGTABLET / ORALAB1988-11-14b8a1b40f171c…
2025-01-19 17:59 UTC · 7 captures of this ZIP2025-01A071655-001OXYBUTYNIN CHLORIDE5MGTABLET / ORALAB1988-11-1403ed91905a0d…
2024-12-13 21:23 UTC · 2 captures of this ZIP2024-12A071655-001OXYBUTYNIN CHLORIDE5MGTABLET / ORALAB1988-11-142680178bc6a6…
2024-09-14 05:58 UTC · 2 captures of this ZIP2024-09A071655-001OXYBUTYNIN CHLORIDE5MGTABLET / ORALAB1988-11-145bbf6a4d5a75…
2024-11-08 22:44 UTC · 3 captures of this ZIP2024-11A071655-001OXYBUTYNIN CHLORIDE5MGTABLET / ORALAB1988-11-14d8e5a09893c0…
2024-10-29 15:01 UTC2024-10A071655-001OXYBUTYNIN CHLORIDE5MGTABLET / ORALAB1988-11-14d06236e962d9…
2024-08-13 05:28 UTC · 3 captures of this ZIP2024-08A071655-001OXYBUTYNIN CHLORIDE5MGTABLET / ORALAB1988-11-1479d66fd596c7…
2024-07-13 05:37 UTC · 2 captures of this ZIP2024-07A071655-001OXYBUTYNIN CHLORIDE5MGTABLET / ORALAB1988-11-14301d65b070ca…
2024-06-18 03:08 UTC · 5 captures of this ZIP2024-06A071655-001OXYBUTYNIN CHLORIDE5MGTABLET / ORALAB1988-11-141e350fbaab3a…
2024-05-31 18:47 UTC2024-05A071655-001OXYBUTYNIN CHLORIDE5MGTABLET / ORALAB1988-11-148072bd15b7f6…
2022-06-29 02:47 UTC · 2 captures of this ZIP2022-06A071655-001OXYBUTYNIN CHLORIDE5MGTABLET / ORALAB1988-11-145c6f7cd8ea54…
2022-04-08 23:34 UTC2022-04A071655-001OXYBUTYNIN CHLORIDE5MGTABLET / ORALAB1988-11-145d02ea3f76ae…
2022-04-04 05:41 UTC2022-04A071655-001OXYBUTYNIN CHLORIDE5MGTABLET / ORALAB1988-11-144b0b4de00fa7…
2019-12-13 00:20 UTC2019-12A071655-001OXYBUTYNIN CHLORIDE5MGTABLET / ORALAB1988-11-1474a2ff9319b5…
2022-03-09 01:35 UTC2022-03A071655-001OXYBUTYNIN CHLORIDE5MGTABLET / ORALAB1988-11-14bb7c543d1eb4…
2021-12-28 21:50 UTC2021-12A071655-001OXYBUTYNIN CHLORIDE5MGTABLET / ORALAB1988-11-14782e0a99824c…
2021-05-05 16:15 UTC · 3 captures of this ZIP2021-05A071655-001OXYBUTYNIN CHLORIDE5MGTABLET / ORALAB1988-11-1487673890dc5c…
2021-03-12 10:30 UTC2021-03A071655-001OXYBUTYNIN CHLORIDE5MGTABLET / ORALAB1988-11-145aa47cf7b7d7…
2020-12-22 03:56 UTC2020-12A071655-001OXYBUTYNIN CHLORIDE5MGTABLET / ORALAB1988-11-148869cabd3fbd…
2020-11-12 02:37 UTC2020-11A071655-001OXYBUTYNIN CHLORIDE5MGTABLET / ORALAB1988-11-14c0c555d07b60…
2019-12-14 00:12 UTC2019-12A071655-001OXYBUTYNIN CHLORIDE5MGTABLET / ORALAB1988-11-143f01610625f2…
2019-09-15 20:21 UTC2019-09A071655-001OXYBUTYNIN CHLORIDE5MGTABLET / ORALAB1988-11-14b00525d2431f…
2019-07-19 19:46 UTC2019-07A071655-001OXYBUTYNIN CHLORIDE5MGTABLET / ORALAB1988-11-14ea99ee380514…
2024-03-16 18:09 UTC · 4 captures of this ZIP2024-03A071655-001OXYBUTYNIN CHLORIDE5MGTABLET / ORALAB1988-11-146a51e52b5d6a…
2024-02-18 07:12 UTC2024-02A071655-001OXYBUTYNIN CHLORIDE5MGTABLET / ORALAB1988-11-141c564ffb4f44…
2023-12-20 04:57 UTC2023-12A071655-001OXYBUTYNIN CHLORIDE5MGTABLET / ORALAB1988-11-14ea1830bbd6c7…
2023-11-28 05:40 UTC · 2 captures of this ZIP2023-11A071655-001OXYBUTYNIN CHLORIDE5MGTABLET / ORALAB1988-11-14a72a2bbeb626…
2023-10-25 00:34 UTC · 2 captures of this ZIP2023-10A071655-001OXYBUTYNIN CHLORIDE5MGTABLET / ORALAB1988-11-149b2671bbb829…
2023-07-15 15:27 UTC · 2 captures of this ZIP2023-07A071655-001OXYBUTYNIN CHLORIDE5MGTABLET / ORALAB1988-11-14a67488948f0b…
2023-06-13 01:57 UTC · 3 captures of this ZIP2023-06A071655-001OXYBUTYNIN CHLORIDE5MGTABLET / ORALAB1988-11-143f0d92c62455…
2023-05-13 08:27 UTC2023-05A071655-001OXYBUTYNIN CHLORIDE5MGTABLET / ORALAB1988-11-14053a50430f4f…
2023-01-26 05:58 UTC2023-01A071655-001OXYBUTYNIN CHLORIDE5MGTABLET / ORALAB1988-11-143bdfa0b2c4d7…
2022-11-12 20:34 UTC · 5 captures of this ZIP2022-11A071655-001OXYBUTYNIN CHLORIDE5MGTABLET / ORALAB1988-11-143a93d1ddd44b…
2022-10-28 04:53 UTC2022-10A071655-001OXYBUTYNIN CHLORIDE5MGTABLET / ORALAB1988-11-14f41ea6bd6efb…

Observed Orange Book normalized TE history#

Normalized TE history page 1 of 2 · 43 observed states.

Captured, Edition, Application-product table
CapturedEditionApplication-productTE codeOrderSource SHA-256
2026-09-14 22:38:342026-08A071655-001AB184e616aacf4f…
2026-08-18 06:07:402026-07A071655-001AB1caaa826d4ba7…
2026-02-19 14:30 UTC2026-02A071655-001AB1011fe1cb6892…
2025-12-14 10:44 UTC · 2 captures of this ZIP2025-12A071655-001AB131067a03dcf5…
2025-08-23 18:47 UTC2025-08A071655-001AB16a471c1ec25d…
2025-03-22 03:13 UTC · 3 captures of this ZIP2025-03A071655-001AB1fd3edfee7708…
2025-02-26 10:13 UTC · 3 captures of this ZIP2025-02A071655-001AB1b8a1b40f171c…
2025-01-19 17:59 UTC · 7 captures of this ZIP2025-01A071655-001AB103ed91905a0d…
2024-12-13 21:23 UTC · 2 captures of this ZIP2024-12A071655-001AB12680178bc6a6…
2024-09-14 05:58 UTC · 2 captures of this ZIP2024-09A071655-001AB15bbf6a4d5a75…
2024-11-08 22:44 UTC · 3 captures of this ZIP2024-11A071655-001AB1d8e5a09893c0…
2024-10-29 15:01 UTC2024-10A071655-001AB1d06236e962d9…
2024-08-13 05:28 UTC · 3 captures of this ZIP2024-08A071655-001AB179d66fd596c7…
2024-07-13 05:37 UTC · 2 captures of this ZIP2024-07A071655-001AB1301d65b070ca…
2024-06-18 03:08 UTC · 5 captures of this ZIP2024-06A071655-001AB11e350fbaab3a…
2024-05-31 18:47 UTC2024-05A071655-001AB18072bd15b7f6…
2022-06-29 02:47 UTC · 2 captures of this ZIP2022-06A071655-001AB15c6f7cd8ea54…
2022-04-08 23:34 UTC2022-04A071655-001AB15d02ea3f76ae…
2022-04-04 05:41 UTC2022-04A071655-001AB14b0b4de00fa7…
2019-12-13 00:20 UTC2019-12A071655-001AB174a2ff9319b5…
2022-03-09 01:35 UTC2022-03A071655-001AB1bb7c543d1eb4…
2021-12-28 21:50 UTC2021-12A071655-001AB1782e0a99824c…
2021-05-05 16:15 UTC · 3 captures of this ZIP2021-05A071655-001AB187673890dc5c…
2021-03-12 10:30 UTC2021-03A071655-001AB15aa47cf7b7d7…
2020-12-22 03:56 UTC2020-12A071655-001AB18869cabd3fbd…
2020-11-12 02:37 UTC2020-11A071655-001AB1c0c555d07b60…
2019-12-14 00:12 UTC2019-12A071655-001AB13f01610625f2…
2019-09-15 20:21 UTC2019-09A071655-001AB1b00525d2431f…
2019-07-19 19:46 UTC2019-07A071655-001AB1ea99ee380514…
2024-03-16 18:09 UTC · 4 captures of this ZIP2024-03A071655-001AB16a51e52b5d6a…
2024-02-18 07:12 UTC2024-02A071655-001AB11c564ffb4f44…
2023-12-20 04:57 UTC2023-12A071655-001AB1ea1830bbd6c7…
2023-11-28 05:40 UTC · 2 captures of this ZIP2023-11A071655-001AB1a72a2bbeb626…
2023-10-25 00:34 UTC · 2 captures of this ZIP2023-10A071655-001AB19b2671bbb829…
2023-07-15 15:27 UTC · 2 captures of this ZIP2023-07A071655-001AB1a67488948f0b…
2023-06-13 01:57 UTC · 3 captures of this ZIP2023-06A071655-001AB13f0d92c62455…
2023-05-13 08:27 UTC2023-05A071655-001AB1053a50430f4f…
2023-01-26 05:58 UTC2023-01A071655-001AB13bdfa0b2c4d7…
2022-11-12 20:34 UTC · 5 captures of this ZIP2022-11A071655-001AB13a93d1ddd44b…
2022-10-28 04:53 UTC2022-10A071655-001AB1f41ea6bd6efb…

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.

Matched openFDA labels page 1 of 1 · 2 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
Oxybutynin ChlorideOXYBUTYNIN CHLORIDETeva Pharmaceuticals USA, Inc.cb7aba8d-6913-4f57-8eb4-c6d6ff0b2a292024-09-02Warnings, Adverse reactionsExact identifier
ndc (product): 50111-456
80e61d72-77a8-4d3f-b251-7b3272351d33d2aa1b90-bea7-4a93-b2e7-22710548ff552010-06-07Warnings, Adverse reactionsExact identifier
spl id: 80e61d72-77a8-4d3f-b251-7b3272351d33
spl set id: d2aa1b90-bea7-4a93-b2e7-22710548ff55

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.