NDC 50090-6199 – Oxybutynin Chloride

Oxybutynin Chloride 5 mg/1 · Tablet · Oral

Human Prescription Drug

Product NDC50090-6199

Product details

Brand name
Oxybutynin Chloride
Generic name
Oxybutynin Chloride
Labeler
A-S Medication Solutions
Dosage form
Tablet
Route
Oral
Marketing category
ANDA · ANDA212798
Marketed since
November 1, 2019
Listing expires
December 31, 2026
Pharmacologic class
Cholinergic Muscarinic Antagonist

Active ingredients

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

Package NDC codes (3)

Package NDCDescriptionSince
50090-6199-030 TABLET in 1 BOTTLE (50090-6199-0)Nov 2, 2022
50090-6199-1100 TABLET in 1 BOTTLE (50090-6199-1)Nov 2, 2022
50090-6199-390 TABLET in 1 BOTTLE (50090-6199-3)Nov 2, 2022

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