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Finasteride

NDC 17856-0090, finasteride, tablet, film coated, from Atlantic Biologicals Corps.

Product NDC
17856-0090
Status
Listed
Labeler
Atlantic Biologicals Corps
Dosage form
TABLET, FILM COATED
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA090121
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/17856-0090 \
  -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
17856-0090-1178560090011 TABLET, FILM COATED in 1 POUCH (17856-0090-1)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/29e59387-120c-4367-9f87-75cb53b6460d

Use it

Look up 17856-0090 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/17856-0090 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 17856-0090. 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.