NDC 60687-899 – Oxybutynin Chloride

Oxybutynin Chloride 5 mg/1 · Tablet · Oral

Human Prescription Drug

Product NDC60687-899

Product details

Brand name
Oxybutynin Chloride
Generic name
Oxybutynin Chloride
Labeler
American Health Packaging
Dosage form
Tablet
Route
Oral
Marketing category
ANDA · ANDA208165
Marketed since
April 16, 2026
Listing expires
December 31, 2027
Pharmacologic class
Cholinergic Muscarinic Antagonist

Active ingredients

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

Package NDC codes (1)

Package NDCDescriptionSince
60687-899-01100 BLISTER PACK in 1 CARTON (60687-899-01) / 1 TABLET in 1 BLISTER PACK (60687-899-11)Apr 16, 2026

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