DailyMed label

fenofibrate

DailyMed label · Leading Pharma, LLC · version 2

Key facts

Product fenofibrate
Labeler Leading Pharma, LLC
Document type HUMAN PRESCRIPTION DRUG LABEL
Active ingredients FENOFIBRATE
Active ingredient UNIIs U202363UOS
Application number 211122
Route ORAL
NDC package codes 69315-287-09, 69315-288-09, 69315-288-05
Effective date Dec 6, 2024
Set ID ca09372a-3c75-47c9-80a3-e08dbe243bb4

At a glance

  • 1–9 NDC package codes
  • 1–9 Active ingredients
  • 1–9 Manufacturing establishments listed

Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.

About DailyMed drug labels

DailyMed publishes the structured product labeling (SPL) that companies submit to the FDA, including package NDCs, ingredients and the establishments that make each product.

Source: U.S. National Library of Medicine (NLM), DailyMed · Source date:

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