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Gemfibrozil

NDC 66267-436, Gemfibrozil, tablet, from NuCare Pharmaceuticals, Inc..

Product NDC
66267-436
Status
Listed
Labeler
NuCare Pharmaceuticals, Inc.
Dosage form
TABLET
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA077836
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/66267-436 \
  -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
66267-436-306626704363030 TABLET in 1 BOTTLE (66267-436-30)
66267-436-606626704366060 TABLET in 1 BOTTLE (66267-436-60)
66267-436-9266267043692180 TABLET in 1 BOTTLE (66267-436-92)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/415ac7e0-ddc7-453e-e054-00144ff8d46c

Use it

Look up 66267-436 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/66267-436 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 66267-436. 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.