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Finasteride

NDC 47335-714, Finasteride, tablet, film coated, from Sun Pharmaceutical Industries, Inc..

Product NDC
47335-714
Status
Listed
Labeler
Sun Pharmaceutical Industries, Inc.
Dosage form
TABLET, FILM COATED
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA090508
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/47335-714 \
  -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
47335-714-0847335071408100 TABLET, FILM COATED in 1 BOTTLE (47335-714-08)
47335-714-18473350714181000 TABLET, FILM COATED in 1 BOTTLE (47335-714-18)
47335-714-814733507148190 TABLET, FILM COATED in 1 BOTTLE (47335-714-81)
47335-714-834733507148330 TABLET, FILM COATED in 1 BOTTLE (47335-714-83)
47335-714-8847335071488100 TABLET, FILM COATED in 1 BOTTLE (47335-714-88)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/abd87058-923f-4767-986c-278201c0e688

Use it

Look up 47335-714 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/47335-714 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 47335-714. 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.