NDC 63629-9689 – Oxybutynin chloride

Oxybutynin Chloride 5 mg/1 · Tablet, Extended Release · Oral

Human Prescription Drug

Product NDC63629-9689

Product details

Brand name
Oxybutynin chloride
Generic name
Oxybutynin chloride
Labeler
Bryant Ranch Prepack
Dosage form
Tablet, Extended Release
Route
Oral
Marketing category
ANDA · ANDA207138
Marketed since
December 14, 2016
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
63629-9689-130 TABLET, EXTENDED RELEASE in 1 BOTTLE (63629-9689-1)Jun 21, 2023
63629-9689-2100 TABLET, EXTENDED RELEASE in 1 BOTTLE (63629-9689-2)Jun 21, 2023

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