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Gemfibrozil

NDC 71335-1902, Gemfibrozil, tablet, from Bryant Ranch Prepack.

Product NDC
71335-1902
Status
Listed
Labeler
Bryant Ranch Prepack
Dosage form
TABLET
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA203266
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/71335-1902 \
  -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
71335-1902-17133519020160 TABLET in 1 BOTTLE (71335-1902-1)
71335-1902-27133519020230 TABLET in 1 BOTTLE (71335-1902-2)
71335-1902-371335190203100 TABLET in 1 BOTTLE (71335-1902-3)
71335-1902-47133519020490 TABLET in 1 BOTTLE (71335-1902-4)
71335-1902-571335190205180 TABLET in 1 BOTTLE (71335-1902-5)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/fe91d458-1877-4c2e-aa15-efd802e6741f

Use it

Look up 71335-1902 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/71335-1902 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 71335-1902. 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.