Oxybutynin Chloride Syrup USP

Manufacturer
Pharmaceutical Associates, Inc.
Effective date
2012-08-03
Label type
HUMAN PRESCRIPTION DRUG LABEL
Version
2
Source
legacy-cache
Hydrated at
2026-08-02 01:46:31

Label at a glance#

ProductOXYBUTYNIN CHLORIDE
Active ingredientOXYBUTYNIN CHLORIDE
Label structure12 sections

Indications and uses

Oxybutynin chloride syrup is 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 teaspoonful (5 mg/5 mL) two to three times a day. The maximum recommended dose is one teaspoonful (5 mg/5 mL) four times a day. Pediatric patients over 5 years of age: The usual dose is one teaspoonful (5 mg/5 mL) two times a day. The maximum recommended dose is one teaspoonful (5 mg/5 mL) three times a day.

Label contents#

Full prescribing information#

DESCRIPTION

DESCRIPTION SECTION

Chemically, oxybutynin chloride is d,l (racemic) 4-diethylamino-2-butynyl phenylcyclohexylglycolate hydrochloride. The molecular formula of oxybutynin chloride is C22H31NO3•HCl. The structural formula appears below:

Chemical Structure
Chemical Structure

Oxybutynin chloride is a white crystalline solid with a molecular weight of 393.96. It is readily soluble in water and acids, but relatively insoluble in alkalis.

Each 5 mL of oxybutynin chloride syrup, for oral administration, contains 5 mg oxybutynin chloride with inactive ingredients citric acid, FD&C Green No. 3, glycerin, methylparaben, cherry flavor, sodium citrate, sorbitol, sucrose, and water.

Therapeutic Category: Antispasmodic, anticholinergic.

CLINICAL PHARMACOLOGY

CLINICAL PHARMACOLOGY SECTION

Oxybutynin chloride exerts direct antispasmodic effect on smooth muscle and inhibits the muscarinic action of acetylcholine on smooth muscle. Oxybutynin chloride 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 chloride relaxes bladder smooth muscle. In patients with conditions characterized by involuntary bladder contractions, cystometric studies have demonstrated that oxybutynin chloride increases bladder (vesical) capacity, diminishes the frequency of uninhibited contractions of the detrusor muscle, and delays the initial desire to void. Oxybutynin chloride 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 2 years. Pharmacokinetic information is not currently available.

INDICATIONS AND USAGE

INDICATIONS & USAGE SECTION

Oxybutynin chloride syrup is 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 chloride.

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 chloride 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 chloride showed no increase of mutagenic activity when tested in Schizosaccharomyces pompholiciformis, Saccharomyces cerevisiae and Salmonella typhimurium test systems. Reproduction studies in the hamster, rabbit, rat, and mouse have shown no definite evidence of impaired fertility.

Pregnancy

PREGNANCY SECTION

Category B

TERATOGENIC EFFECTS SECTION

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 chloride 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 pediatric patients 5 years of age and older (see DOSAGE AND ADMINISTRATION). However, as there is insufficient clinical data for pediatric populations under age 5, oxybutynin chloride 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, vasodilation

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, and 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 teaspoonful (5 mg/5 mL) two to three times a day. The maximum recommended dose is one teaspoonful (5 mg/5 mL) four times a day.

Pediatric patients over 5 years of age: The usual dose is one teaspoonful (5 mg/5 mL) two times a day. The maximum recommended dose is one teaspoonful (5 mg/5 mL) three times a day.

HOW SUPPLIED

HOW SUPPLIED SECTION

Oxybutynin Chloride Syrup USP (5 mg/5 mL) is a cherry flavored, blue liquid supplied in bottles of 16 fluid ounces (473 mL) (NDC 0121- 0671-16) and 5 mL Unit Dose Cups (NDC 0121-0671-05).

STORAGE AND HANDLING SECTION

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

Store at controlled room temperature, 15° to 30°C (59° to 86°F).

SPL UNCLASSIFIED SECTION

Rx ONLY

Manufactured By:

Pharmaceutical
Associates, Inc.

Greenville, SC 29605

R01/99

PRINCIPAL DISPLAY PANEL - 473 mL Bottle Label

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

NDC 0121-0671-16

Oxybutynin Chloride
Syrup USP
5 mg/5 mL

Each teaspoonful (5 mL) contains:
5 mg oxybutynin chloride.

Rx ONLY

16 fl oz (473 mL)

pai
Pharmaceutical
Associates, Inc.

Greenville, SC 29605

PRINCIPAL DISPLAY PANEL - 473 mL Bottle Label
PRINCIPAL DISPLAY PANEL - 473 mL Bottle Label

FDA-Initiated Inactive NDC Indexing#

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDCBilling unitProduct NDCDailyMed indexing SPLSPL versionEffective
0121-0671-05ML - Milliliter0121-0671c8badb82-4b8c-4172-9196-61ca8804472e12013-02-13
0121-0671-16ML - Milliliter0121-06718ec85f95-5e3d-4ace-9f7b-398d22f7afe312013-02-13

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
IngredientTypeUNIISPL versionUploaded
OXYBUTYNIN CHLORIDEACTIVE INGREDIENTL9F3D9RENQ2
OXYBUTYNINACTIVE MOIETYK9P6MC70922
CITRIC ACID MONOHYDRATEINACTIVE INGREDIENT2968PHW8QP2
FD&C GREEN NO. 3INACTIVE INGREDIENT3P3ONR6O1S2
GLYCERININACTIVE INGREDIENTPDC6A3C0OX2
METHYLPARABENINACTIVE INGREDIENTA2I8C7HI9T2
SODIUM CITRATEINACTIVE INGREDIENT1Q73Q2JULR2
SORBITOLINACTIVE INGREDIENT506T60A25R2
SUCROSEINACTIVE INGREDIENTC151H8M5542
WATERINACTIVE INGREDIENT059QF0KO0R2

Products#

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

DailyMed product names page 1 of 1 · 10 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
0121-06710121-0671-16, 0121-0671-05

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 9 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 6 · 349 matching rows.

DailyMed ingredient, IID ingredient, UNII table
DailyMed ingredientIID ingredientUNIIDosage form / routePotencyMaximum daily exposureMatch
METHYLPARABENMETHYLPARABENA2I8C7HI9TINJECTION / INTRALESIONAL0.15 %w/vExact identifier — unii candidate
79 equally ranked IID candidates
CITRIC ACID MONOHYDRATECITRIC ACID MONOHYDRATE2968PHW8QPSHAMPOO / TOPICAL17 mgExact identifier — unii candidate
88 equally ranked IID candidates
CITRIC ACID MONOHYDRATECITRIC ACID MONOHYDRATE2968PHW8QPCREAM / TOPICAL4 mgExact identifier — unii candidate
88 equally ranked IID candidates
GLYCERINGLYCERINPDC6A3C0OXSOLUTION, CONCENTRATE / ORAL200 mg/1mlExact identifier — unii candidate
75 equally ranked IID candidates
METHYLPARABENMETHYLPARABENA2I8C7HI9TSPRAY / TOPICAL0.2 %w/wExact identifier — unii candidate
79 equally ranked IID candidates
CITRIC ACID MONOHYDRATECITRIC ACID MONOHYDRATE2968PHW8QPINJECTION, POWDER, FOR SOLUTION / INTRAVENOUS608 mgExact identifier — unii candidate
88 equally ranked IID candidates
SORBITOLSORBITOL506T60A25RTABLET / SUBLINGUAL50.5 mgExact identifier — unii candidate
44 equally ranked IID candidates
CITRIC ACID MONOHYDRATECITRIC ACID MONOHYDRATE2968PHW8QPEMULSION / TOPICAL0.11 %w/wExact identifier — unii candidate
88 equally ranked IID candidates
SUCROSESUCROSEC151H8M554SOLUTION / RECTAL35.42 %w/vExact identifier — unii candidate
48 equally ranked IID candidates
CITRIC ACID MONOHYDRATECITRIC ACID MONOHYDRATE2968PHW8QPSUSPENSION / OPHTHALMICADJ PHExact identifier — unii candidate
88 equally ranked IID candidates
GLYCERINGLYCERINPDC6A3C0OXCLOTH / TOPICAL0.05 mg/mgExact identifier — unii candidate
75 equally ranked IID candidates
FD&C GREEN NO. 3FD&C GREEN NO. 33P3ONR6O1SCAPSULE, EXTENDED RELEASE / ORAL0.16 mgExact identifier — unii candidate
15 equally ranked IID candidates
CITRIC ACID MONOHYDRATECITRIC ACID MONOHYDRATE2968PHW8QPLOTION / TOPICAL0.85 %w/wExact identifier — unii candidate
88 equally ranked IID candidates
GLYCERINGLYCERINPDC6A3C0OXINJECTION, SOLUTION / INTRAMUSCULAR15 %w/vExact identifier — unii candidate
75 equally ranked IID candidates
METHYLPARABENMETHYLPARABENA2I8C7HI9TAEROSOL, FOAM / VAGINAL0.1 %w/wExact identifier — unii candidate
79 equally ranked IID candidates
METHYLPARABENMETHYLPARABENA2I8C7HI9TCONCENTRATE / ORAL12 mgExact identifier — unii candidate
79 equally ranked IID candidates
SUCROSESUCROSEC151H8M554TROCHE / ORALNAExact identifier — unii candidate
48 equally ranked IID candidates
GLYCERINGLYCERINPDC6A3C0OXSYRUP / ORAL16734 mgExact identifier — unii candidate
75 equally ranked IID candidates
SUCROSESUCROSEC151H8M554INJECTION, SUSPENSION, LIPOSOMAL / INTRAVENOUS9.4 %w/vExact identifier — unii candidate
48 equally ranked IID candidates
GLYCERINGLYCERINPDC6A3C0OXSPONGE / TOPICAL2 %w/wExact identifier — unii candidate
75 equally ranked IID candidates
SUCROSESUCROSEC151H8M554TABLET, CHEWABLE / ORAL7258 mgExact identifier — unii candidate
48 equally ranked IID candidates
METHYLPARABENMETHYLPARABENA2I8C7HI9TTABLET, EXTENDED RELEASE / ORAL0.17 mgExact identifier — unii candidate
79 equally ranked IID candidates
SUCROSESUCROSEC151H8M554GRANULE / ORALNAExact identifier — unii candidate
48 equally ranked IID candidates
METHYLPARABENMETHYLPARABENA2I8C7HI9TINJECTION / INFILTRATION80 mgExact identifier — unii candidate
79 equally ranked IID candidates
CITRIC ACID MONOHYDRATECITRIC ACID MONOHYDRATE2968PHW8QPSOAP / TOPICAL0.5 %w/wExact identifier — unii candidate
88 equally ranked IID candidates
GLYCERINGLYCERINPDC6A3C0OXTABLET, EXTENDED RELEASE / ORAL7 mgExact identifier — unii candidate
75 equally ranked IID candidates
CITRIC ACID MONOHYDRATECITRIC ACID MONOHYDRATE2968PHW8QPSOLUTION / INTRAVENOUS10 mgExact identifier — unii candidate
88 equally ranked IID candidates
SUCROSESUCROSEC151H8M554SOLUTION / ORAL70000 mgExact identifier — unii candidate
48 equally ranked IID candidates
CITRIC ACID MONOHYDRATECITRIC ACID MONOHYDRATE2968PHW8QPINJECTION / INTRAVENOUS2068 mgExact identifier — unii candidate
88 equally ranked IID candidates
GLYCERINGLYCERINPDC6A3C0OXSOLUTION/ DROPS / AURICULAR (OTIC)25 mgExact identifier — unii candidate
75 equally ranked IID candidates
GLYCERINGLYCERINPDC6A3C0OXSUSPENSION / OPHTHALMIC58 mgExact identifier — unii candidate
75 equally ranked IID candidates
FD&C GREEN NO. 3FD&C GREEN NO. 33P3ONR6O1SCAPSULE / ORAL40 mgExact identifier — unii candidate
15 equally ranked IID candidates
SUCROSESUCROSEC151H8M554SUSPENSION/ DROPS / ORAL3750 mgExact identifier — unii candidate
48 equally ranked IID candidates
SUCROSESUCROSEC151H8M554GRANULE, FOR SUSPENSION / ORAL31885 mgExact identifier — unii candidate
48 equally ranked IID candidates
SUCROSESUCROSEC151H8M554TABLET / ORAL4249 mgExact identifier — unii candidate
48 equally ranked IID candidates
SORBITOLSORBITOL506T60A25RTABLET, CHEWABLE / ORAL3555 mgExact identifier — unii candidate
44 equally ranked IID candidates
METHYLPARABENMETHYLPARABENA2I8C7HI9TSOLUTION / NASAL250 mgExact identifier — unii candidate
79 equally ranked IID candidates
CITRIC ACID MONOHYDRATECITRIC ACID MONOHYDRATE2968PHW8QPFILM, EXTENDED RELEASE / TRANSDERMAL1.38 mgExact identifier — unii candidate
88 equally ranked IID candidates
GLYCERINGLYCERINPDC6A3C0OXTABLET, COATED / ORAL1 mgExact identifier — unii candidate
75 equally ranked IID candidates
CITRIC ACID MONOHYDRATECITRIC ACID MONOHYDRATE2968PHW8QPOINTMENT / TOPICAL1 mgExact identifier — unii candidate
88 equally ranked IID candidates
SUCROSESUCROSEC151H8M554SUPPOSITORY / RECTALNAExact identifier — unii candidate
48 equally ranked IID candidates
CITRIC ACID MONOHYDRATECITRIC ACID MONOHYDRATE2968PHW8QPPOWDER, FOR SOLUTION / ORAL315 mgExact identifier — unii candidate
88 equally ranked IID candidates
CITRIC ACID MONOHYDRATECITRIC ACID MONOHYDRATE2968PHW8QPSOLUTION / OPHTHALMIC0.03 %w/vExact identifier — unii candidate
88 equally ranked IID candidates
METHYLPARABENMETHYLPARABENA2I8C7HI9TINJECTION / PARENTERAL18 mgExact identifier — unii candidate
79 equally ranked IID candidates
GLYCERINGLYCERINPDC6A3C0OXGEL / TRANSDERMAL500 mgExact identifier — unii candidate
75 equally ranked IID candidates
SORBITOLSORBITOL506T60A25RINJECTION / INTRASYNOVIAL45 %w/vExact identifier — unii candidate
44 equally ranked IID candidates
GLYCERINGLYCERINPDC6A3C0OXSUSPENSION, EXTENDED RELEASE / ORAL2000 mgExact identifier — unii candidate
75 equally ranked IID candidates
SUCROSESUCROSEC151H8M554CAPSULE, DELAYED RELEASE / ORAL955 mgExact identifier — unii candidate
48 equally ranked IID candidates
GLYCERINGLYCERINPDC6A3C0OXSUSPENSION / AURICULAR (OTIC)0.05 %w/wExact identifier — unii candidate
75 equally ranked IID candidates
SORBITOLSORBITOL506T60A25RSOLUTION / ORAL29268 mgExact identifier — unii candidate
44 equally ranked IID candidates
CITRIC ACID MONOHYDRATECITRIC ACID MONOHYDRATE2968PHW8QPSPRAY / NASAL9 mgExact identifier — unii candidate
88 equally ranked IID candidates
METHYLPARABENMETHYLPARABENA2I8C7HI9TFILM, SOLUBLE / BUCCAL3 mgExact identifier — unii candidate
79 equally ranked IID candidates
SUCROSESUCROSEC151H8M554POWDER, FOR SUSPENSION / ORAL40017 mgExact identifier — unii candidate
48 equally ranked IID candidates
METHYLPARABENMETHYLPARABENA2I8C7HI9TINJECTION, SOLUTION / PARENTERAL30 mgExact identifier — unii candidate
79 equally ranked IID candidates
CITRIC ACID MONOHYDRATECITRIC ACID MONOHYDRATE2968PHW8QPINJECTION / SOFT TISSUEADJ PHExact identifier — unii candidate
88 equally ranked IID candidates
METHYLPARABENMETHYLPARABENA2I8C7HI9TCREAM / TOPICAL3000 mgExact identifier — unii candidate
79 equally ranked IID candidates
CITRIC ACID MONOHYDRATECITRIC ACID MONOHYDRATE2968PHW8QPTROCHE / ORAL12 mgExact identifier — unii candidate
88 equally ranked IID candidates
METHYLPARABENMETHYLPARABENA2I8C7HI9TINJECTION, SUSPENSION / SUBCUTANEOUS0.16 %w/vExact identifier — unii candidate
79 equally ranked IID candidates
FD&C GREEN NO. 3FD&C GREEN NO. 33P3ONR6O1SSHAMPOO / TOPICAL0.09 %w/wExact identifier — unii candidate
15 equally ranked IID candidates
CITRIC ACID MONOHYDRATECITRIC ACID MONOHYDRATE2968PHW8QPCAPSULE, EXTENDED RELEASE / ORAL101 mgExact identifier — unii candidate
88 equally ranked IID candidates

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 44.

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
A075137-001OXYBUTYNIN CHLORIDEOXYBUTYNIN CHLORIDE5MG/5MLSYRUP / ORAL1998-12-18

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 · 44 observed states.

Captured, Edition, Application-product table
CapturedEditionApplication-productTrade nameStrengthDosage form / routeProduct TE source textRLD / RSApproval dateSource SHA-256
2026-10-15 13:18:302026-09A075137-001OXYBUTYNIN CHLORIDE5MG/5MLSYRUP / ORAL1998-12-18c2088c7a36db…
2026-09-14 22:38:342026-08A075137-001OXYBUTYNIN CHLORIDE5MG/5MLSYRUP / ORAL1998-12-1884e616aacf4f…
2026-08-18 06:07:402026-07A075137-001OXYBUTYNIN CHLORIDE5MG/5MLSYRUP / ORAL1998-12-18caaa826d4ba7…
2026-02-19 14:30 UTC2026-02A075137-001OXYBUTYNIN CHLORIDE5MG/5MLSYRUP / ORAL1998-12-18011fe1cb6892…
2025-12-14 10:44 UTC · 2 captures of this ZIP2025-12A075137-001OXYBUTYNIN CHLORIDE5MG/5MLSYRUP / ORAL1998-12-1831067a03dcf5…
2025-08-23 18:47 UTC2025-08A075137-001OXYBUTYNIN CHLORIDE5MG/5MLSYRUP / ORAL1998-12-186a471c1ec25d…
2025-03-22 03:13 UTC · 3 captures of this ZIP2025-03A075137-001OXYBUTYNIN CHLORIDE5MG/5MLSYRUP / ORAL1998-12-18fd3edfee7708…
2025-02-26 10:13 UTC · 3 captures of this ZIP2025-02A075137-001OXYBUTYNIN CHLORIDE5MG/5MLSYRUP / ORAL1998-12-18b8a1b40f171c…
2025-01-19 17:59 UTC · 7 captures of this ZIP2025-01A075137-001OXYBUTYNIN CHLORIDE5MG/5MLSYRUP / ORAL1998-12-1803ed91905a0d…
2024-12-13 21:23 UTC · 2 captures of this ZIP2024-12A075137-001OXYBUTYNIN CHLORIDE5MG/5MLSYRUP / ORAL1998-12-182680178bc6a6…
2024-09-14 05:58 UTC · 2 captures of this ZIP2024-09A075137-001OXYBUTYNIN CHLORIDE5MG/5MLSYRUP / ORAL1998-12-185bbf6a4d5a75…
2024-11-08 22:44 UTC · 3 captures of this ZIP2024-11A075137-001OXYBUTYNIN CHLORIDE5MG/5MLSYRUP / ORAL1998-12-18d8e5a09893c0…
2024-10-29 15:01 UTC2024-10A075137-001OXYBUTYNIN CHLORIDE5MG/5MLSYRUP / ORAL1998-12-18d06236e962d9…
2024-08-13 05:28 UTC · 3 captures of this ZIP2024-08A075137-001OXYBUTYNIN CHLORIDE5MG/5MLSYRUP / ORAL1998-12-1879d66fd596c7…
2024-07-13 05:37 UTC · 2 captures of this ZIP2024-07A075137-001OXYBUTYNIN CHLORIDE5MG/5MLSYRUP / ORAL1998-12-18301d65b070ca…
2024-06-18 03:08 UTC · 5 captures of this ZIP2024-06A075137-001OXYBUTYNIN CHLORIDE5MG/5MLSYRUP / ORAL1998-12-181e350fbaab3a…
2024-05-31 18:47 UTC2024-05A075137-001OXYBUTYNIN CHLORIDE5MG/5MLSYRUP / ORAL1998-12-188072bd15b7f6…
2022-06-29 02:47 UTC · 2 captures of this ZIP2022-06A075137-001OXYBUTYNIN CHLORIDE5MG/5MLSYRUP / ORALAA1998-12-185c6f7cd8ea54…
2022-04-08 23:34 UTC2022-04A075137-001OXYBUTYNIN CHLORIDE5MG/5MLSYRUP / ORALAA1998-12-185d02ea3f76ae…
2022-04-04 05:41 UTC2022-04A075137-001OXYBUTYNIN CHLORIDE5MG/5MLSYRUP / ORALAA1998-12-184b0b4de00fa7…
2019-12-13 00:20 UTC2019-12A075137-001OXYBUTYNIN CHLORIDE5MG/5MLSYRUP / ORALAA1998-12-1874a2ff9319b5…
2022-03-09 01:35 UTC2022-03A075137-001OXYBUTYNIN CHLORIDE5MG/5MLSYRUP / ORALAA1998-12-18bb7c543d1eb4…
2021-12-28 21:50 UTC2021-12A075137-001OXYBUTYNIN CHLORIDE5MG/5MLSYRUP / ORALAA1998-12-18782e0a99824c…
2021-05-05 16:15 UTC · 3 captures of this ZIP2021-05A075137-001OXYBUTYNIN CHLORIDE5MG/5MLSYRUP / ORALAA1998-12-1887673890dc5c…
2021-03-12 10:30 UTC2021-03A075137-001OXYBUTYNIN CHLORIDE5MG/5MLSYRUP / ORALAA1998-12-185aa47cf7b7d7…
2020-12-22 03:56 UTC2020-12A075137-001OXYBUTYNIN CHLORIDE5MG/5MLSYRUP / ORALAA1998-12-188869cabd3fbd…
2020-11-12 02:37 UTC2020-11A075137-001OXYBUTYNIN CHLORIDE5MG/5MLSYRUP / ORALAA1998-12-18c0c555d07b60…
2019-12-14 00:12 UTC2019-12A075137-001OXYBUTYNIN CHLORIDE5MG/5MLSYRUP / ORALAA1998-12-183f01610625f2…
2019-09-15 20:21 UTC2019-09A075137-001OXYBUTYNIN CHLORIDE5MG/5MLSYRUP / ORALAA1998-12-18b00525d2431f…
2019-07-19 19:46 UTC2019-07A075137-001OXYBUTYNIN CHLORIDE5MG/5MLSYRUP / ORALAA1998-12-18ea99ee380514…
2024-03-16 18:09 UTC · 4 captures of this ZIP2024-03A075137-001OXYBUTYNIN CHLORIDE5MG/5MLSYRUP / ORAL1998-12-186a51e52b5d6a…
2024-02-18 07:12 UTC2024-02A075137-001OXYBUTYNIN CHLORIDE5MG/5MLSYRUP / ORALAA1998-12-181c564ffb4f44…
2023-12-20 04:57 UTC2023-12A075137-001OXYBUTYNIN CHLORIDE5MG/5MLSYRUP / ORALAA1998-12-18ea1830bbd6c7…
2023-11-28 05:40 UTC · 2 captures of this ZIP2023-11A075137-001OXYBUTYNIN CHLORIDE5MG/5MLSYRUP / ORALAA1998-12-18a72a2bbeb626…
2023-10-25 00:34 UTC · 2 captures of this ZIP2023-10A075137-001OXYBUTYNIN CHLORIDE5MG/5MLSYRUP / ORALAA1998-12-189b2671bbb829…
2023-07-15 15:27 UTC · 2 captures of this ZIP2023-07A075137-001OXYBUTYNIN CHLORIDE5MG/5MLSYRUP / ORALAA1998-12-18a67488948f0b…
2023-06-13 01:57 UTC · 3 captures of this ZIP2023-06A075137-001OXYBUTYNIN CHLORIDE5MG/5MLSYRUP / ORALAA1998-12-183f0d92c62455…
2023-05-13 08:27 UTC2023-05A075137-001OXYBUTYNIN CHLORIDE5MG/5MLSYRUP / ORALAA1998-12-18053a50430f4f…
2023-01-26 05:58 UTC2023-01A075137-001OXYBUTYNIN CHLORIDE5MG/5MLSYRUP / ORALAA1998-12-183bdfa0b2c4d7…
2022-11-12 20:34 UTC · 5 captures of this ZIP2022-11A075137-001OXYBUTYNIN CHLORIDE5MG/5MLSYRUP / ORALAA1998-12-183a93d1ddd44b…

Observed Orange Book normalized TE history#

Captured, Edition, Application-product table
CapturedEditionApplication-productTE codeOrderSource SHA-256
2022-06-29 02:47 UTC · 2 captures of this ZIP2022-06A075137-001AA15c6f7cd8ea54…
2022-04-08 23:34 UTC2022-04A075137-001AA15d02ea3f76ae…
2022-04-04 05:41 UTC2022-04A075137-001AA14b0b4de00fa7…
2019-12-13 00:20 UTC2019-12A075137-001AA174a2ff9319b5…
2022-03-09 01:35 UTC2022-03A075137-001AA1bb7c543d1eb4…
2021-12-28 21:50 UTC2021-12A075137-001AA1782e0a99824c…
2021-05-05 16:15 UTC · 3 captures of this ZIP2021-05A075137-001AA187673890dc5c…
2021-03-12 10:30 UTC2021-03A075137-001AA15aa47cf7b7d7…
2020-12-22 03:56 UTC2020-12A075137-001AA18869cabd3fbd…
2020-11-12 02:37 UTC2020-11A075137-001AA1c0c555d07b60…
2019-12-14 00:12 UTC2019-12A075137-001AA13f01610625f2…
2019-09-15 20:21 UTC2019-09A075137-001AA1b00525d2431f…
2019-07-19 19:46 UTC2019-07A075137-001AA1ea99ee380514…
2024-02-18 07:12 UTC2024-02A075137-001AA11c564ffb4f44…
2023-12-20 04:57 UTC2023-12A075137-001AA1ea1830bbd6c7…
2023-11-28 05:40 UTC · 2 captures of this ZIP2023-11A075137-001AA1a72a2bbeb626…
2023-10-25 00:34 UTC · 2 captures of this ZIP2023-10A075137-001AA19b2671bbb829…
2023-07-15 15:27 UTC · 2 captures of this ZIP2023-07A075137-001AA1a67488948f0b…
2023-06-13 01:57 UTC · 3 captures of this ZIP2023-06A075137-001AA13f0d92c62455…
2023-05-13 08:27 UTC2023-05A075137-001AA1053a50430f4f…
2023-01-26 05:58 UTC2023-01A075137-001AA13bdfa0b2c4d7…
2022-11-12 20:34 UTC · 5 captures of this ZIP2022-11A075137-001AA13a93d1ddd44b…
2022-10-28 04:53 UTC2022-10A075137-001AA1f41ea6bd6efb…
2022-09-29 23:25 UTC2022-09A075137-001AA1e64feba35796…
2022-07-09 03:26 UTC · 3 captures of this ZIP2022-07A075137-001AA1cb3db0bc1861…

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 · 1 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
efa6c082-a729-e0d0-e053-2995a90a74461c6dfc08-b177-41eb-9865-368252a1b8bb2022-12-12Warnings, Adverse reactionsExact identifier
spl set id: 1c6dfc08-b177-41eb-9865-368252a1b8bb

Reported adverse events (FAERS/openFDA)#

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