NDC 62135-509 – Oxybutynin chloride

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

Human Prescription Drug

Product NDC62135-509

Product details

Brand name
Oxybutynin chloride
Generic name
Oxybutynin Chloride
Labeler
Chartwell RX, LLC
Dosage form
Tablet, Extended Release
Route
Oral
Marketing category
ANDA · ANDA078503
Marketed since
March 1, 2009
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
62135-509-9090 TABLET, EXTENDED RELEASE in 1 BOTTLE (62135-509-90)Mar 3, 2023

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