NDC 50268-627 – Oxybutynin Chloride Extended Release

Oxybutynin Chloride 5 mg/1 · Tablet, Extended Release · Oral

Human Prescription Drug

Product NDC50268-627

Product details

Brand name
Oxybutynin Chloride Extended Release
Generic name
Oxybutynin Chloride
Labeler
AvPAK
Dosage form
Tablet, Extended Release
Route
Oral
Marketing category
ANDA · ANDA078503
Marketed since
May 25, 2012
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
50268-627-1550 BLISTER PACK in 1 BOX (50268-627-15) / 1 TABLET, EXTENDED RELEASE in 1 BLISTER PACK (50268-627-11)May 25, 2012

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