NDC 67046-1600 – Oxybutynin Chloride

Oxybutynin Chloride 15 mg/1 · Tablet, Extended Release · Oral

Human Prescription Drug

Product NDC67046-1600

Product details

Brand name
Oxybutynin Chloride
Generic name
Oxybutynin Chloride
Labeler
Coupler LLC
Dosage form
Tablet, Extended Release
Route
Oral
Marketing category
ANDA · ANDA211655
Marketed since
September 23, 2025
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
67046-1600-330 TABLET, EXTENDED RELEASE in 1 BLISTER PACK (67046-1600-3)Sep 23, 2025

Other Oxybutynin Chloride products