NDC 70710-1127 – Ursodiol

Ursodiol 250 mg/1 · Tablet · Oral

Human Prescription Drug

Product NDC70710-1127

Product details

Brand name
Ursodiol
Generic name
Ursodiol
Labeler
Zydus Pharmaceuticals (USA) Inc.
Dosage form
Tablet
Route
Oral
Marketing category
ANDA · ANDA211145
Marketed since
November 7, 2018
Listing expires
December 31, 2026
Pharmacologic class
Bile Acid

Active ingredients

Uses, dosage, side effects and warnings for Ursodiol →

Package NDC codes (2)

Package NDCDescriptionSince
70710-1127-1100 TABLET in 1 BOTTLE (70710-1127-1)Nov 7, 2018
70710-1127-5500 TABLET in 1 BOTTLE (70710-1127-5)Nov 7, 2018

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