NDC 72789-414 – Oxybutynin Chloride Extended Release

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

Human Prescription Drug

Product NDC72789-414

Product details

Brand name
Oxybutynin Chloride Extended Release
Generic name
Oxybutynin Chloride
Labeler
PD-Rx Pharmaceuticals, Inc.
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
72789-414-9090 TABLET, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (72789-414-90)Jun 11, 2024

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