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Finasteride

NDC 55111-171, Finasteride, tablet, film coated, from Dr. Reddy's Laboratories Limited.

Product NDC
55111-171
Status
Listed
Labeler
Dr. Reddy's Laboratories Limited
Dosage form
TABLET, FILM COATED
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA076436
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/55111-171 \
  -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
55111-171-0555111017105500 TABLET, FILM COATED in 1 BOTTLE (55111-171-05)
55111-171-1855111017118180 TABLET, FILM COATED in 1 BOTTLE (55111-171-18)
55111-171-305511101713030 TABLET, FILM COATED in 1 BOTTLE (55111-171-30)
55111-171-905511101719090 TABLET, FILM COATED in 1 BOTTLE (55111-171-90)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/fa19372d-027d-a91b-f58e-1bdb8fd7e2b6

Use it

Look up 55111-171 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/55111-171 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 55111-171. 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.