NDC 71610-394 – Oxybutynin Chloride

Oxybutynin Chloride 5 mg/1 · Tablet · Oral

Human Prescription Drug

Product NDC71610-394

Product details

Brand name
Oxybutynin Chloride
Generic name
oxybutynin chloride
Labeler
Aphena Pharma Solutions - Tennessee, LLC
Dosage form
Tablet
Route
Oral
Marketing category
ANDA · ANDA210125
Marketed since
January 1, 2019
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
71610-394-5360 TABLET in 1 BOTTLE, PLASTIC (71610-394-53)Feb 5, 2020
71610-394-6090 TABLET in 1 BOTTLE, PLASTIC (71610-394-60)Feb 5, 2020
71610-394-80180 TABLET in 1 BOTTLE, PLASTIC (71610-394-80)Dec 30, 2022
71610-394-92270 TABLET in 1 BOTTLE, PLASTIC (71610-394-92)Feb 5, 2020

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