NDC 63629-2287 – Ursodiol

Ursodiol 500 mg/1 · Tablet, Film Coated · Oral

Human Prescription Drug

Product NDC63629-2287

Product details

Brand name
Ursodiol
Generic name
Ursodiol
Labeler
Bryant Ranch Prepack
Dosage form
Tablet, Film Coated
Route
Oral
Marketing category
ANDA · ANDA202540
Marketed since
August 1, 2013
Listing expires
December 31, 2026
Pharmacologic class
Bile Acid

Active ingredients

Uses, dosage, side effects and warnings for Ursodiol →

Package NDC codes (1)

Package NDCDescriptionSince
63629-2287-1100 TABLET, FILM COATED in 1 BOTTLE (63629-2287-1)Mar 29, 2021

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