NDC 51655-665 – Oxybutynin Chloride

Oxybutynin Chloride 5 mg/1 · Tablet · Oral

Human Prescription Drug

Product NDC51655-665

Product details

Brand name
Oxybutynin Chloride
Generic name
Oxybutynin Chloride
Labeler
Northwind Health Company, LLC
Dosage form
Tablet
Route
Oral
Marketing category
ANDA · ANDA209823
Marketed since
August 9, 2022
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
51655-665-2560 TABLET in 1 BOTTLE, PLASTIC (51655-665-25)Dec 16, 2022
51655-665-5230 TABLET in 1 BOTTLE, PLASTIC (51655-665-52)Aug 9, 2022

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