NDC 43353-282 – Oxybutynin Chloride Extended Release

Oxybutynin Chloride 5 mg/1 · Tablet, Extended Release · Oral

Human Prescription Drug

Product NDC43353-282

Product details

Brand name
Oxybutynin Chloride Extended Release
Generic name
Oxybutynin Chloride
Labeler
Aphena Pharma Solutions - Tennessee, LLC
Dosage form
Tablet, Extended Release
Route
Oral
Marketing category
ANDA · ANDA078503
Marketed since
March 9, 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 (4)

Package NDCDescriptionSince
43353-282-3030 TABLET, EXTENDED RELEASE in 1 BOTTLE (43353-282-30)Mar 2, 2017
43353-282-5360 TABLET, EXTENDED RELEASE in 1 BOTTLE (43353-282-53)Mar 2, 2017
43353-282-6090 TABLET, EXTENDED RELEASE in 1 BOTTLE (43353-282-60)Mar 2, 2017
43353-282-80180 TABLET, EXTENDED RELEASE in 1 BOTTLE (43353-282-80)May 31, 2023

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