NDC 23155-810 – Oxybutynin Chloride

Oxybutynin Chloride 5 mg/1 · Tablet · Oral

Human Prescription Drug

Product NDC23155-810

Product details

Brand name
Oxybutynin Chloride
Generic name
Oxybutynin Chloride
Labeler
Heritage Pharmaceuticals Inc. d/b/a Avet Pharmaceuticals Inc.
Dosage form
Tablet
Route
Oral
Marketing category
ANDA · ANDA208165
Marketed since
January 31, 2022
Marketing end
August 31, 2027
Pharmacologic class
Cholinergic Muscarinic Antagonist

Active ingredients

Uses, dosage, side effects and warnings for Oxybutynin Chloride →

Package NDC codes (3)

Package NDCDescriptionSince
23155-810-01100 TABLET in 1 BOTTLE (23155-810-01)Jan 31, 2022
23155-810-05500 TABLET in 1 BOTTLE (23155-810-05)Jan 31, 2022
23155-810-101000 TABLET in 1 BOTTLE (23155-810-10)Jan 31, 2022

Other Oxybutynin Chloride products