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Ursodiol

NDC 63629-2287, Ursodiol, tablet, film coated, from Bryant Ranch Prepack.

Product NDC
63629-2287
Status
Listed
Labeler
Bryant Ranch Prepack
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/63629-2287 \
  -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
63629-2287-163629228701100 TABLET, FILM COATED in 1 BOTTLE (63629-2287-1)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/5e6ced5f-b8ef-4e6b-a7c1-730bac650c5b

Use it

Look up 63629-2287 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/63629-2287 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 63629-2287. 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.