NDC 50090-6967 – Oxybutynin Chloride

Oxybutynin Chloride 5 mg/1 · Tablet · Oral

Human Prescription Drug

Product NDC50090-6967

Product details

Brand name
Oxybutynin Chloride
Generic name
Oxybutynin Chloride
Labeler
A-S Medication Solutions
Dosage form
Tablet
Route
Oral
Marketing category
ANDA · ANDA209823
Marketed since
November 15, 2017
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
50090-6967-090 TABLET in 1 BOTTLE (50090-6967-0)Dec 21, 2023

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