NDC 16729-317 – Oxybutynin chloride

Oxybutynin Chloride 5 mg/1 · Tablet, Extended Release · Oral

Human Prescription Drug

Product NDC16729-317

Product details

Brand name
Oxybutynin chloride
Generic name
Oxybutynin chloride
Labeler
Accord Healthcare, Inc.
Dosage form
Tablet, Extended Release
Route
Oral
Marketing category
ANDA · ANDA207138
Marketed since
December 14, 2016
Listing expires
December 31, 2026
Pharmacologic class
Cholinergic Muscarinic Antagonist

Active ingredients

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

Package NDC codes (2)

Package NDCDescriptionSince
16729-317-01100 TABLET, EXTENDED RELEASE in 1 BOTTLE (16729-317-01)Dec 14, 2016
16729-317-16500 TABLET, EXTENDED RELEASE in 1 BOTTLE (16729-317-16)Mar 30, 2017

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