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Finasteride

NDC 35573-400, Finasteride, tablet, film coated, from Burel Pharmaceuticals, LLC.

Product NDC
35573-400
Status
Listed
Labeler
Burel Pharmaceuticals, LLC
Dosage form
TABLET, FILM COATED
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA203687
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/35573-400 \
  -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
35573-400-99355730400991000 TABLET, FILM COATED in 1 BOTTLE (35573-400-99)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/c8516eaa-98d0-4eb1-bc65-aa765baea5db

  • NADAC price for package 35573040099

    GET /v1/drugs/nadac/35573040099

Use it

Look up 35573-400 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/35573-400 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 35573-400. 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.