NDC 71610-277 – Oxybutynin Chloride

Oxybutynin Chloride 5 mg/1 · Tablet · Oral

Human Prescription Drug

Product NDC71610-277

Product details

Brand name
Oxybutynin Chloride
Generic name
Oxybutynin Chloride
Labeler
Aphena Pharma Solutions - Tennessee, LLC
Dosage form
Tablet
Route
Oral
Marketing category
ANDA · ANDA209823
Marketed since
October 23, 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 (5)

Package NDCDescriptionSince
71610-277-3030 TABLET in 1 BOTTLE (71610-277-30)May 31, 2023
71610-277-5360 TABLET in 1 BOTTLE (71610-277-53)May 13, 2019
71610-277-6090 TABLET in 1 BOTTLE (71610-277-60)May 13, 2019
71610-277-80180 TABLET in 1 BOTTLE (71610-277-80)May 13, 2019
71610-277-92270 TABLET in 1 BOTTLE (71610-277-92)May 13, 2019

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