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Fenofibrate

NDC 71205-949, Fenofibrate, tablet, film coated, from Proficient Rx LP.

Product NDC
71205-949
Status
Listed
Labeler
Proficient Rx LP
Dosage form
TABLET, FILM COATED
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA207803
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/71205-949 \
  -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
71205-949-307120509493030 TABLET, FILM COATED in 1 BOTTLE (71205-949-30)
71205-949-5571205094955500 TABLET, FILM COATED in 1 BOTTLE (71205-949-55)
71205-949-607120509496060 TABLET, FILM COATED in 1 BOTTLE (71205-949-60)
71205-949-7271205094972120 TABLET, FILM COATED in 1 BOTTLE (71205-949-72)
71205-949-7871205094978180 TABLET, FILM COATED in 1 BOTTLE (71205-949-78)
71205-949-907120509499090 TABLET, FILM COATED in 1 BOTTLE (71205-949-90)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/41f0f514-1fa9-47a0-a085-a31354842f96

Use it

Look up 71205-949 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/71205-949 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 71205-949. 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.