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GEMFIBROZIL

NDC 68788-7964, Gemfibrozil, tablet, from Preferred Pharmaceuticals, Inc..

Product NDC
68788-7964
Status
Listed
Labeler
Preferred 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/68788-7964 \
  -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
68788-7964-36878879640330 TABLET in 1 BOTTLE (68788-7964-3)
68788-7964-66878879640660 TABLET in 1 BOTTLE (68788-7964-6)
68788-7964-96878879640990 TABLET in 1 BOTTLE (68788-7964-9)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/2f5738ac-1c9c-4f3a-8c7d-6039d768831e

Use it

Look up 68788-7964 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/68788-7964 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 68788-7964. 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.