NDC 52817-260 – Oxybutynin Chloride

Oxybutynin Chloride 5 mg/1 · Tablet · Oral

Human Prescription Drug

Product NDC52817-260

Product details

Brand name
Oxybutynin Chloride
Generic name
Oxybutynin chloride
Labeler
TruPharma LLC
Dosage form
Tablet
Route
Oral
Marketing category
ANDA · ANDA210125
Marketed since
January 1, 2019
Listing expires
December 31, 2027
Pharmacologic class
Cholinergic Muscarinic Antagonist

Active ingredients

Uses, dosage, side effects and warnings for Oxybutynin Chloride →

Package NDC codes (2)

Package NDCDescriptionSince
52817-260-10100 TABLET in 1 BOTTLE, PLASTIC (52817-260-10)Jan 1, 2019
52817-260-50500 TABLET in 1 BOTTLE, PLASTIC (52817-260-50)Jan 1, 2019

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