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Ursodiol

NDC 0904-6890, Ursodiol, tablet, film coated, from Major Pharmaceuticals.

Product NDC
0904-6890
Status
Listed
Labeler
Major Pharmaceuticals
Dosage form
TABLET, FILM COATED
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA202540
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/0904-6890 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • URSODIOL250 mg/1

Pharmacologic classes

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

Package NDCNDC-11Package
0904-6890-040090468900430 BLISTER PACK in 1 CARTON (0904-6890-04) / 1 TABLET, FILM COATED in 1 BLISTER PACK

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/e1f6abfd-2158-4824-b53d-717fbe6de3f9
  • NADAC price for package 00904689004

    GET /v1/drugs/nadac/00904689004

Use it

Look up 0904-6890 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/0904-6890 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 0904-6890. Tell me the product, its labeler, dosage form and route, its packages, and the RxNorm concepts it maps to.

Source: FDA, release 2026-10-23. Public domain. Reference data, not medical advice.