NDC 54838-510 – Oxybutynin Chloride

Oxybutynin Chloride 5 mg/5mL · Syrup · Oral

Human Prescription Drug

Product NDC54838-510

Product details

Brand name
Oxybutynin Chloride
Generic name
Oxybutynin Chloride
Labeler
Lannett Company, Inc.
Dosage form
Syrup
Route
Oral
Marketing category
ANDA · ANDA074520
Marketed since
March 29, 1996
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
54838-510-80473 mL in 1 BOTTLE, PLASTIC (54838-510-80)Mar 29, 1996

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