NDC 16729-319 – Oxybutynin chloride

Oxybutynin Chloride 15 mg/1 · Tablet, Extended Release · Oral

Human Prescription Drug

Product NDC16729-319

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 (1)

Package NDCDescriptionSince
16729-319-01100 TABLET, EXTENDED RELEASE in 1 BOTTLE (16729-319-01)Dec 14, 2016

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