NDC 66267-642 – Oxybutynin Chloride

Oxybutynin Chloride 5 mg/1 · Tablet · Oral

Human Prescription Drug

Product NDC66267-642

Product details

Brand name
Oxybutynin Chloride
Generic name
Oxybutynin Chloride
Labeler
NuCare Pharmaceuticals,Inc.
Dosage form
Tablet
Route
Oral
Marketing category
ANDA · ANDA209823
Marketed since
November 15, 2017
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
66267-642-3030 TABLET in 1 BOTTLE (66267-642-30)Jul 25, 2019

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