NDC 71335-1014 – Oxybutynin Chloride

Oxybutynin Chloride 5 mg/1 · Tablet · Oral

Human Prescription Drug

Product NDC71335-1014

Product details

Brand name
Oxybutynin Chloride
Generic name
Oxybutynin Chloride
Labeler
Bryant Ranch Prepack
Dosage form
Tablet
Route
Oral
Marketing category
ANDA · ANDA209025
Marketed since
February 1, 2018
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
71335-1014-130 TABLET in 1 BOTTLE (71335-1014-1)Nov 21, 2018
71335-1014-2100 TABLET in 1 BOTTLE (71335-1014-2)Aug 9, 2024
71335-1014-320 TABLET in 1 BOTTLE (71335-1014-3)Aug 9, 2024
71335-1014-460 TABLET in 1 BOTTLE (71335-1014-4)Aug 9, 2024
71335-1014-590 TABLET in 1 BOTTLE (71335-1014-5)Aug 9, 2024
71335-1014-642 TABLET in 1 BOTTLE (71335-1014-6)Aug 9, 2024
71335-1014-715 TABLET in 1 BOTTLE (71335-1014-7)Aug 9, 2024
71335-1014-8180 TABLET in 1 BOTTLE (71335-1014-8)Aug 9, 2024

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