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Fenofibrate

NDC 68788-8106, Fenofibrate, tablet, film coated, from Preferred Pharmaceuticals, Inc..

Product NDC
68788-8106
Status
Listed
Labeler
Preferred Pharmaceuticals, Inc.
Dosage form
TABLET, FILM COATED
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA204598
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/68788-8106 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • FENOFIBRATE145 mg/1

Pharmacologic classes

Peroxisome Proliferator Receptor alpha Agonist [EPC]

Package NDCNDC-11Package
68788-8106-168788810601100 TABLET, FILM COATED in 1 BOTTLE (68788-8106-1)
68788-8106-36878881060330 TABLET, FILM COATED in 1 BOTTLE (68788-8106-3)
68788-8106-66878881060660 TABLET, FILM COATED in 1 BOTTLE (68788-8106-6)
68788-8106-96878881060990 TABLET, FILM COATED in 1 BOTTLE (68788-8106-9)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/c810b16b-32e2-4d0c-aa28-bf1f62110757

Use it

Look up 68788-8106 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/68788-8106 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 68788-8106. 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.