NDC 27241-156 – Oxybutynin Chloride

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

Human Prescription Drug

Product NDC27241-156

Product details

Brand name
Oxybutynin Chloride
Generic name
Oxybutynin Chloride
Labeler
Ajanta Pharma USA Inc.
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 (2)

Package NDCDescriptionSince
27241-156-04100 TABLET, EXTENDED RELEASE in 1 BOTTLE (27241-156-04)Feb 28, 2019
27241-156-08500 TABLET, EXTENDED RELEASE in 1 BOTTLE (27241-156-08)Feb 28, 2019

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