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Ursodiol

NDC 70771-1408, Ursodiol, tablet, from Zydus Lifesciences Limited.

Product NDC
70771-1408
Status
Listed
Labeler
Zydus Lifesciences Limited
Dosage form
TABLET
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA211145
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/70771-1408 \
  -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
70771-1408-170771140801100 TABLET in 1 BOTTLE (70771-1408-1)
70771-1408-570771140805500 TABLET in 1 BOTTLE (70771-1408-5)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/792d8b51-3815-44d2-a20e-b494a9d0e055

Use it

Look up 70771-1408 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/70771-1408 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 70771-1408. 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.