NDC 72189-132 – Oxybutynin Chloride

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

Human Prescription Drug

Product NDC72189-132

Product details

Brand name
Oxybutynin Chloride
Generic name
Oxybutynin Chloride
Labeler
DIRECT RX
Dosage form
Tablet, Extended Release
Route
Oral
Marketing category
ANDA · ANDA207138
Marketed since
August 24, 2020
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
72189-132-3030 TABLET, EXTENDED RELEASE in 1 BOTTLE (72189-132-30)Aug 24, 2020

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