NDC 0904-6890 – Ursodiol

Ursodiol 250 mg/1 · Tablet, Film Coated · Oral

Human Prescription Drug

Product NDC0904-6890

Product details

Brand name
Ursodiol
Generic name
Ursodiol
Labeler
Major Pharmaceuticals
Dosage form
Tablet, Film Coated
Route
Oral
Marketing category
ANDA · ANDA202540
Marketed since
August 1, 2013
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
0904-6890-0430 BLISTER PACK in 1 CARTON (0904-6890-04) / 1 TABLET, FILM COATED in 1 BLISTER PACKAug 1, 2013

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