NDC 68001-377 – Ursodiol

Ursodiol 250 mg/1 · Tablet · Oral

Human Prescription Drug

Product NDC68001-377

Product details

Brand name
Ursodiol
Generic name
Ursodiol
Labeler
BluePoint Laboratories
Dosage form
Tablet
Route
Oral
Marketing category
ANDA · ANDA090801
Marketed since
February 26, 2019
Listing expires
December 31, 2027
Pharmacologic class
Bile Acid

Active ingredients

Uses, dosage, side effects and warnings for Ursodiol →

Package NDC codes (1)

Package NDCDescriptionSince
68001-377-00100 TABLET in 1 BOTTLE (68001-377-00)Feb 26, 2019

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