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Gemfibrozil

NDC 70518-4764, Gemfibrozil, tablet, film coated, from REMEDYREPACK INC..

Product NDC
70518-4764
Status
Listed
Labeler
REMEDYREPACK INC.
Dosage form
TABLET, FILM COATED
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA202726
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/70518-4764 \
  -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
70518-4764-07051847640030 TABLET, FILM COATED in 1 BLISTER PACK (70518-4764-0)

Linked data

RxNorm, label and prices

RxNorm concepts

RxNorm links no concept to this product's packages.

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/cf32b795-bf42-4861-b273-06d27de3f21d

Use it

Look up 70518-4764 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/70518-4764 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 70518-4764. 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.