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FENOFIBRATE

NDC 70756-214, FENOFIBRATE, tablet, from Lifestar Pharma LLC.

Product NDC
70756-214
Status
Listed
Labeler
Lifestar Pharma LLC
Dosage form
TABLET
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA213864
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/70756-214 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • FENOFIBRATE54 mg/1

Pharmacologic classes

Peroxisome Proliferator Receptor alpha Agonist [EPC]

Package NDCNDC-11Package
70756-214-5170756021451500 TABLET in 1 BOTTLE (70756-214-51)
70756-214-907075602149090 TABLET in 1 BOTTLE (70756-214-90)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/1da57e8c-3977-43e1-aa7e-229760203f7d

  • NADAC price for package 70756021451

    GET /v1/drugs/nadac/70756021451

  • NADAC price for package 70756021490

    GET /v1/drugs/nadac/70756021490

Use it

Look up 70756-214 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/70756-214 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 70756-214. 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.