NDC 0832-0038 – Oxybutynin Chloride

Oxybutynin Chloride 5 mg/1 · Tablet · Oral

Human Prescription Drug

Product NDC0832-0038

Product details

Brand name
Oxybutynin Chloride
Generic name
Oxybutynin Chloride
Labeler
Upsher-Smith Laboratories, LLC
Dosage form
Tablet
Route
Oral
Marketing category
ANDA · ANDA074625
Marketed since
November 7, 2011
Marketing end
December 31, 2028
Pharmacologic class
Cholinergic Muscarinic Antagonist

Active ingredients

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

Package NDC codes (3)

Package NDCDescriptionSince
0832-0038-00100 TABLET in 1 BOTTLE (0832-0038-00)Nov 7, 2011
0832-0038-101000 TABLET in 1 BOTTLE (0832-0038-10)Nov 7, 2011
0832-0038-50500 TABLET in 1 BOTTLE (0832-0038-50)Nov 7, 2011

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