NDC 72888-032 – Oxybutynin Chloride

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

Human Prescription Drug

Product NDC72888-032

Product details

Brand name
Oxybutynin Chloride
Generic name
Oxybutynin Chloride
Labeler
Advagen Pharma Limited
Dosage form
Tablet, Extended Release
Route
Oral
Marketing category
ANDA · ANDA214415
Marketed since
October 27, 2020
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
72888-032-01100 TABLET, EXTENDED RELEASE in 1 BOTTLE (72888-032-01)Oct 27, 2020
72888-032-05500 TABLET, EXTENDED RELEASE in 1 BOTTLE (72888-032-05)Jul 10, 2024

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