NDC 71610-860 – Oxybutynin Chloride

Oxybutynin Chloride 5 mg/1 · Tablet · Oral

Human Prescription Drug

Product NDC71610-860

Product details

Brand name
Oxybutynin Chloride
Generic name
Oxybutynin chloride
Labeler
Aphena Pharma Solutions - Tennessee, LLC
Dosage form
Tablet
Route
Oral
Marketing category
ANDA · ANDA075079
Marketed since
September 30, 2022
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
71610-860-3030 TABLET in 1 BOTTLE (71610-860-30)Oct 10, 2024
71610-860-5360 TABLET in 1 BOTTLE (71610-860-53)Oct 10, 2024
71610-860-6090 TABLET in 1 BOTTLE (71610-860-60)Oct 10, 2024
71610-860-80180 TABLET in 1 BOTTLE (71610-860-80)Oct 10, 2024

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