NDC 82868-047 – Oxybutynin Chloride

Oxybutynin Chloride 5 mg/1 · Tablet · Oral

Human Prescription Drug

Product NDC82868-047

Product details

Brand name
Oxybutynin Chloride
Generic name
Oxybutynin Chloride
Labeler
Northwind Health Company, LLC
Dosage form
Tablet
Route
Oral
Marketing category
ANDA · ANDA209335
Marketed since
February 19, 2024
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
82868-047-3030 TABLET in 1 BOTTLE, PLASTIC (82868-047-30)Feb 19, 2024

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