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Ursodiol

NDC 68462-474, Ursodiol, tablet, from Glenmark Pharmaceuticals Inc., USA.

Product NDC
68462-474
Status
Listed
Labeler
Glenmark Pharmaceuticals Inc., USA
Dosage form
TABLET
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA090801
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/68462-474 \
  -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
68462-474-0168462047401100 TABLET in 1 BOTTLE (68462-474-01)
68462-474-0568462047405500 TABLET in 1 BOTTLE (68462-474-05)
68462-474-306846204743030 TABLET in 1 BOTTLE (68462-474-30)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/fb79b62a-b450-4d7a-be28-5ee4d174fd58

  • NADAC price for package 68462047401

    GET /v1/drugs/nadac/68462047401

Use it

Look up 68462-474 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/68462-474 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 68462-474. 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.