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Urso Forte

NDC 58914-790, Ursodiol, tablet, film coated, from Allergan, Inc..

Product NDC
58914-790
Status
Listed
Labeler
Allergan, Inc.
Dosage form
TABLET, FILM COATED
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
NDA
Application
NDA020675
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/58914-790 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • URSODIOL500 mg/1

Pharmacologic classes

Bile Acid [EPC]; Bile Acids and Salts [CS]

Package NDCNDC-11Package
58914-790-01589140790014 TABLET, FILM COATED in 1 BLISTER PACK (58914-790-01)
58914-790-1058914079010100 TABLET, FILM COATED in 1 BOTTLE (58914-790-10)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/e8fc4fc2-fe5c-4cba-b6e0-5ceaf2157a61

Use it

Look up 58914-790 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/58914-790 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 58914-790. Tell me the product, its labeler, dosage form and route, its packages, and the RxNorm concepts it maps to.
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Source: FDA, release 2026-10-23. Public domain. Reference data, not medical advice.