NDC 67046-1381 – Oxybutynin Chloride

Oxybutynin Chloride 5 mg/1 · Tablet · Oral

Human Prescription Drug

Product NDC67046-1381

Product details

Brand name
Oxybutynin Chloride
Generic name
Oxybutynin Chloride
Labeler
Coupler LLC
Dosage form
Tablet
Route
Oral
Marketing category
ANDA · ANDA208165
Marketed since
July 6, 2026
Marketing end
August 31, 2027
Pharmacologic class
Cholinergic Muscarinic Antagonist

Active ingredients

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

Package NDC codes (1)

Package NDCDescriptionSince
67046-1381-330 TABLET in 1 BLISTER PACK (67046-1381-3)Jul 6, 2026

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