NDC 82804-095 – Oxybutynin Chloride Extended Release

Oxybutynin Chloride 10 mg/1 · Tablet, Extended Release · Oral

Human Prescription Drug

Product NDC82804-095

Product details

Brand name
Oxybutynin Chloride Extended Release
Generic name
Oxybutynin Chloride
Labeler
Proficient Rx LP
Dosage form
Tablet, Extended Release
Route
Oral
Marketing category
ANDA · ANDA206121
Marketed since
September 27, 2016
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
82804-095-3030 TABLET, EXTENDED RELEASE in 1 BOTTLE (82804-095-30)Apr 2, 2024

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