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Oxybutynin - Medication Information

Product NDC Code 70771-1088
Drug Name

Oxybutynin

Type Generic
Pharm Class Cholinergic Muscarinic Antagonist [EPC],
Cholinergic Muscarinic Antagonists [MoA]
Active Ingredients
Oxybutynin chloride 15 mg/1
Route ORAL
Dosage Form TABLET, FILM COATED, EXTENDED RELEASE
RxCUI drug identifier 863619,
863628,
863636
Application Number ANDA202332
Labeler Name Zydus Lifesciences Limited
Packages
Package NDC Code Description
70771-1088-1 100 tablet, film coated, extended release in 1 bottle (70771-1088-1)
70771-1088-3 30 tablet, film coated, extended release in 1 bottle (70771-1088-3)
70771-1088-4 10 blister pack in 1 carton (70771-1088-4) / 10 tablet, film coated, extended release in 1 blister pack (70771-1088-2)
70771-1088-5 500 tablet, film coated, extended release in 1 bottle (70771-1088-5)
70771-1088-6 60 tablet, film coated, extended release in 1 bottle (70771-1088-6)
70771-1088-9 90 tablet, film coated, extended release in 1 bottle (70771-1088-9)
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Spl product data elements

Usually a list of ingredients in a drug product.
oxybutynin oxybutynin OXYBUTYNIN CHLORIDE OXYBUTYNIN ALGINIC ACID HYDROGENATED CASTOR OIL HYPROMELLOSES LACTOSE MONOHYDRATE MAGNESIUM STEARATE METHACRYLIC ACID CELLULOSE, MICROCRYSTALLINE POVIDONE TALC TRIETHYL CITRATE WHITE TO OFF-WHITE ROUND 255 oxybutynin oxybutynin OXYBUTYNIN CHLORIDE OXYBUTYNIN ALGINIC ACID HYDROGENATED CASTOR OIL HYPROMELLOSES LACTOSE MONOHYDRATE MAGNESIUM STEARATE METHACRYLIC ACID CELLULOSE, MICROCRYSTALLINE POVIDONE TALC TRIETHYL CITRATE WHITE TO OFF-WHITE ROUND 256 oxybutynin oxybutynin OXYBUTYNIN CHLORIDE OXYBUTYNIN ALGINIC ACID HYDROGENATED CASTOR OIL HYPROMELLOSES LACTOSE MONOHYDRATE MAGNESIUM STEARATE METHACRYLIC ACID CELLULOSE, MICROCRYSTALLINE POVIDONE TALC TRIETHYL CITRATE WHITE TO OFF-WHITE ROUND 257

Package label principal display panel

The content of the principal display panel of the product package, usually including the product’s name, dosage forms, and other key information about the drug product.
PACKAGE LABEL.PRINCIPAL DISPLAY PANEL Oxybutynin chloride extended-release tablets USP, 5 mg NDC 70771-1086-1 100 tablets Rx only Oxybutynin chloride extended-release tablets USP, 10 mg NDC 70771-1087-1 100 tablets Rx only Oxybutynin chloride extended-release tablets USP, 15 mg NDC 70771-1088-1 100 tablets Rx only Oxybutynin chloride extended-release tablets Oxybutynin chloride extended-release tablets Oxybutynin chloride extended-release tablets

Disclaimer: Do not rely on openFDA or Phanrmacy Near Me to make decisions regarding medical care. While we make every effort to ensure that data is accurate, you should assume all results are unvalidated. Source: OpenFDA, Healthporta Drugs API