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Finasteride

NDC 70518-3182, Finasteride, tablet, film coated, from REMEDYREPACK INC..

Product NDC
70518-3182
Status
Listed
Labeler
REMEDYREPACK INC.
Dosage form
TABLET, FILM COATED
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA090061
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/70518-3182 \
  -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
70518-3182-07051831820030 POUCH in 1 BOX (70518-3182-0) / 1 TABLET, FILM COATED in 1 POUCH (70518-3182-1)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/c2875bc7-e811-4860-9131-da06cecc2137

Use it

Look up 70518-3182 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/70518-3182 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 70518-3182. 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.