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GEMFIBROZIL

NDC 68071-2387, Gemfibrozil, tablet, from NuCare Pharmaceuticals,Inc..

Product NDC
68071-2387
Status
Listed
Labeler
NuCare Pharmaceuticals,Inc.
Dosage form
TABLET
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA214603
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/68071-2387 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • GEMFIBROZIL600 mg/1

Pharmacologic classes

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

Package NDCNDC-11Package
68071-2387-36807123870330 TABLET in 1 BOTTLE (68071-2387-3)
68071-2387-66807123870660 TABLET in 1 BOTTLE (68071-2387-6)
68071-2387-868071238708180 TABLET in 1 BOTTLE (68071-2387-8)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/bfddc3bd-c2dc-449e-e053-2a95a90a8adc

Use it

Look up 68071-2387 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/68071-2387 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 68071-2387. Tell me the product, its labeler, dosage form and route, its packages, and the RxNorm concepts it maps to.

Source: FDA, release 2026-10-23. Public domain. Reference data, not medical advice.