NDC 63187-749 – Oxybutynin Chloride

Oxybutynin Chloride 5 mg/1 · Tablet · Oral

Human Prescription Drug

Product NDC63187-749

Product details

Brand name
Oxybutynin Chloride
Generic name
Oxybutynin Chloride
Labeler
Proficient Rx LP
Dosage form
Tablet
Route
Oral
Marketing category
ANDA · ANDA071655
Marketed since
September 30, 1990
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
63187-749-3030 TABLET in 1 BOTTLE (63187-749-30)Oct 3, 2016
63187-749-6060 TABLET in 1 BOTTLE (63187-749-60)Oct 3, 2016
63187-749-9090 TABLET in 1 BOTTLE (63187-749-90)Oct 3, 2016

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