DailyMed label

Fenofibrate

DailyMed label · Amneal Pharmaceuticals of New York LLC · version 48

Key facts

Product Fenofibrate
Labeler Amneal Pharmaceuticals of New York LLC
Document type HUMAN PRESCRIPTION DRUG LABEL
Active ingredients FENOFIBRATE
Active ingredient UNIIs U202363UOS
Application number 075868
Route ORAL
NDC package codes 0115-0511-01, 0115-0522-01, 0115-0522-02, 0115-0533-01, 0115-0533-02
Effective date Sep 7, 2022
Set ID bfc6668c-3f69-4dd3-bc19-0d26c23dd04c

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.

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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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