NDC 71335-0519 – Oxybutynin Chloride

Oxybutynin Chloride 5 mg/1 · Tablet · Oral

Human Prescription Drug

Product NDC71335-0519

Product details

Brand name
Oxybutynin Chloride
Generic name
Oxybutynin Chloride
Labeler
Bryant Ranch Prepack
Dosage form
Tablet
Route
Oral
Marketing category
ANDA · ANDA071655
Marketed since
September 30, 1990
Listing expires
December 31, 2026
Pharmacologic class
Cholinergic Muscarinic Antagonist

Active ingredients

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

Package NDC codes (8)

Package NDCDescriptionSince
71335-0519-130 TABLET in 1 BOTTLE (71335-0519-1)Jul 22, 2008
71335-0519-2100 TABLET in 1 BOTTLE (71335-0519-2)Jul 22, 2008
71335-0519-320 TABLET in 1 BOTTLE (71335-0519-3)Jul 22, 2008
71335-0519-460 TABLET in 1 BOTTLE (71335-0519-4)Jul 22, 2008
71335-0519-590 TABLET in 1 BOTTLE (71335-0519-5)Jul 22, 2008
71335-0519-642 TABLET in 1 BOTTLE (71335-0519-6)Jul 22, 2008
71335-0519-715 TABLET in 1 BOTTLE (71335-0519-7)Jul 22, 2008
71335-0519-8180 TABLET in 1 BOTTLE (71335-0519-8)Jul 22, 2008

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