NDC 50090-5822 – Oxybutynin chloride

Oxybutynin Chloride 5 mg/1 · Tablet, Extended Release · Oral

Human Prescription Drug

Product NDC50090-5822

Product details

Brand name
Oxybutynin chloride
Generic name
Oxybutynin chloride
Labeler
A-S Medication Solutions
Dosage form
Tablet, Extended Release
Route
Oral
Marketing category
ANDA · ANDA207138
Marketed since
December 14, 2016
Listing expires
December 31, 2026
Pharmacologic class
Cholinergic Muscarinic Antagonist

Active ingredients

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

Package NDC codes (2)

Package NDCDescriptionSince
50090-5822-090 TABLET, EXTENDED RELEASE in 1 BOTTLE (50090-5822-0)Oct 20, 2021
50090-5822-130 TABLET, EXTENDED RELEASE in 1 BOTTLE (50090-5822-1)Jul 19, 2023

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