United States · FDA National Drug Code directory
Urso Forte
A source-listed medicine record.
Factual source checks only. This page is not a clinically reviewed monograph. Historical or discontinued records may be included; listing does not confirm approval, current availability or pharmacy stock.
Medicine identity
- Source reference
- 58914-790_06904c03-cea9-4532-8e27-7f2246be613b
- Product NDC
- 58914-790
- Form
- TABLET, FILM COATED
- Composition / generic term
- Ursodiol
- Labeler
- Allergan, Inc.
- Marketing category
- NDA
- Marketing start / end (source format)
- 19971210
- Source listing expiry
- 20261231
Source-listed ingredients
- URSODIOL — 500 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 4 TABLET, FILM COATED in 1 BLISTER PACK (58914-790-01) · 58914-790-01
- 100 TABLET, FILM COATED in 1 BOTTLE (58914-790-10) · 58914-790-10
Source and coverage
Open FDA National Drug Code directory →
Snapshot retrieved: 2026-09-17. This is the acquisition date, not a medical review date.
Clinical information, images and comparisons appear only when separately reviewed for this record. Coverage may be incomplete. Ask a pharmacist or clinician about your treatment.
Browse United States records →