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FENOFIBRATE

NDC 68788-7816, FENOFIBRATE, tablet, from Preferred Pharmaceuticals Inc..

Product NDC
68788-7816
Status
Listed
Labeler
Preferred Pharmaceuticals Inc.
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/68788-7816 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • FENOFIBRATE160 mg/1

Pharmacologic classes

Peroxisome Proliferator Receptor alpha Agonist [EPC]

Package NDCNDC-11Package
68788-7816-36878878160330 TABLET in 1 BOTTLE (68788-7816-3)
68788-7816-96878878160960 TABLET in 1 BOTTLE (68788-7816-9)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/e573b3f1-5a4c-4a19-9f0f-ee797b379a08

Use it

Look up 68788-7816 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/68788-7816 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 68788-7816. 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.