DailyMed label

Pomalidomide

DailyMed label · Breckenridge Pharmaceutical, Inc. · version 10

Key facts

Product Pomalidomide
Labeler Breckenridge Pharmaceutical, Inc.
Document type HUMAN PRESCRIPTION DRUG LABEL
Active ingredients Pomalidomide
Active ingredient UNIIs D2UX06XLB5
Application number 210111
Route ORAL
NDC package codes 51991-342-21, 51991-342-01, 51991-343-21, 51991-343-01, 51991-344-21, 51991-344-01, 51991-346-21, 51991-346-01
Effective date Mar 4, 2026
Set ID 41400b90-b64e-447b-90f3-1cad58050eba

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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