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Gemfibrozil

NDC 16714-101, gemfibrozil, tablet, from Northstar RxLLC.

Product NDC
16714-101
Status
Listed
Labeler
Northstar RxLLC
Dosage form
TABLET
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA079072
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/16714-101 \
  -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
16714-101-021671401010260 TABLET in 1 BOTTLE (16714-101-02)
16714-101-0516714010105500 TABLET in 1 BOTTLE (16714-101-05)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/75cac02c-56e3-4dfe-b1e2-4ce166b28833

  • NADAC price for package 16714010102

    GET /v1/drugs/nadac/16714010102

  • NADAC price for package 16714010105

    GET /v1/drugs/nadac/16714010105

Use it

Look up 16714-101 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/16714-101 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 16714-101. 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.