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GEMFIBROZIL

NDC 71335-0051, GEMFIBROZIL, tablet, from Bryant Ranch Prepack.

Product NDC
71335-0051
Status
Listed
Labeler
Bryant Ranch Prepack
Dosage form
TABLET
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA078012
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/71335-0051 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • GEMFIBROZIL600 mg/1

Pharmacologic classes

PPAR alpha [CS]; Peroxisome Proliferator Receptor alpha Agonist [EPC]; Peroxisome Proliferator-activated Receptor alpha Agonists [MoA]

Package NDCNDC-11Package
71335-0051-17133500510160 TABLET in 1 BOTTLE (71335-0051-1)
71335-0051-27133500510230 TABLET in 1 BOTTLE (71335-0051-2)
71335-0051-371335005103100 TABLET in 1 BOTTLE (71335-0051-3)
71335-0051-47133500510490 TABLET in 1 BOTTLE (71335-0051-4)
71335-0051-571335005105180 TABLET in 1 BOTTLE (71335-0051-5)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/2cb2de4d-8261-46d8-ae63-c572fdc887d4

Use it

Look up 71335-0051 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/71335-0051 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 71335-0051. 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.