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Gemfibrozil

NDC 50268-350, Gemfibrozil, tablet, from AvPAK.

Product NDC
50268-350
Status
Listed
Labeler
AvPAK
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/50268-350 \
  -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
50268-350-155026803501550 BLISTER PACK in 1 BOX (50268-350-15) / 1 TABLET in 1 BLISTER PACK (50268-350-11)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/3ebb5947-1fe5-9740-6a4b-1f8b577b2711

  • NADAC price for package 50268035015

    GET /v1/drugs/nadac/50268035015

Use it

Look up 50268-350 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/50268-350 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 50268-350. 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.