NDC 68462-474 – Ursodiol

Ursodiol 500 mg/1 · Tablet · Oral

Human Prescription Drug

Product NDC68462-474

Product details

Brand name
Ursodiol
Generic name
Ursodiol
Labeler
Glenmark Pharmaceuticals Inc., USA
Dosage form
Tablet
Route
Oral
Marketing category
ANDA · ANDA090801
Marketed since
July 12, 2011
Listing expires
December 31, 2027
Pharmacologic class
Bile Acid

Active ingredients

Uses, dosage, side effects and warnings for Ursodiol →

Package NDC codes (3)

Package NDCDescriptionSince
68462-474-01100 TABLET in 1 BOTTLE (68462-474-01)Jul 12, 2011
68462-474-05500 TABLET in 1 BOTTLE (68462-474-05)Jul 12, 2011
68462-474-3030 TABLET in 1 BOTTLE (68462-474-30)Jul 12, 2011

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