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Finasteride

NDC 71713-099, Finasteride, tablet, from Thirty Madison Inc.

Product NDC
71713-099
Status
Listed
Labeler
Thirty Madison Inc
Dosage form
TABLET
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA207750
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/71713-099 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • FINASTERIDE1 mg/1

Pharmacologic classes

5-alpha Reductase Inhibitor [EPC]; 5-alpha Reductase Inhibitors [MoA]

Package NDCNDC-11Package
71713-099-907171300999090 TABLET in 1 CONTAINER (71713-099-90)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/3fe7bdaa-b027-4da9-94ee-550bf28c63e1

Use it

Look up 71713-099 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/71713-099 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 71713-099. 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.