United States · FDA National Drug Code directory
Ursodiol 200 mg
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
- 72887-143_c28d41e2-14c2-4401-87ab-49b32239caba
- Product NDC
- 72887-143
- Form
- CAPSULE
- Composition / generic term
- Ursodiol
- Labeler
- FH2 Pharma LLC
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20211118
- Source listing expiry
- 20261231
Source-listed ingredients
- URSODIOL — 200 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 60 CAPSULE in 1 BOTTLE (72887-143-06) · 72887-143-06
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 →