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Finasteride

NDC 76420-154, Finasteride, tablet, film coated, from Asclemed USA, Inc..

Product NDC
76420-154
Status
Listed
Labeler
Asclemed USA, Inc.
Dosage form
TABLET, FILM COATED
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA078341
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/76420-154 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • FINASTERIDE5 mg/1

Pharmacologic classes

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

Package NDCNDC-11Package
76420-154-307642001543030 TABLET, FILM COATED in 1 BOTTLE (76420-154-30)
76420-154-907642001549090 TABLET, FILM COATED in 1 BOTTLE (76420-154-90)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/bafe8674-b7ee-47b2-94c1-842164ca6fa1

Use it

Look up 76420-154 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/76420-154 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 76420-154. 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.