NDC 71335-1690 – Oxybutynin Chloride

Oxybutynin Chloride 10 mg/1 · Tablet, Extended Release · Oral

Human Prescription Drug

Product NDC71335-1690

Product details

Brand name
Oxybutynin Chloride
Generic name
Oxybutynin Chloride
Labeler
Bryant Ranch Prepack
Dosage form
Tablet, Extended Release
Route
Oral
Marketing category
ANDA · ANDA211655
Marketed since
February 28, 2019
Listing expires
December 31, 2027
Pharmacologic class
Cholinergic Muscarinic Antagonist

Active ingredients

Uses, dosage, side effects and warnings for Oxybutynin Chloride →

Package NDC codes (4)

Package NDCDescriptionSince
71335-1690-130 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-1690-1)Dec 29, 2021
71335-1690-218 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-1690-2)Dec 29, 2021
71335-1690-390 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-1690-3)Aug 11, 2020
71335-1690-460 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-1690-4)Dec 29, 2021

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