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Gemfibrozil

NDC 51655-143, Gemfibrozil, tablet, from Northwind Health Company, LLC.

Product NDC
51655-143
Status
Listed
Labeler
Northwind Health Company, LLC
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/51655-143 \
  -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
51655-143-255165501432560 TABLET in 1 BOTTLE, PLASTIC (51655-143-25)
51655-143-265165501432690 TABLET in 1 BOTTLE, PLASTIC (51655-143-26)
51655-143-525165501435230 TABLET in 1 BOTTLE, PLASTIC (51655-143-52)
51655-143-8351655014383180 TABLET in 1 BOTTLE, PLASTIC (51655-143-83)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/a95264ab-eb86-7699-e053-2995a90a3d1f

Use it

Look up 51655-143 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/51655-143 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 51655-143. 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.