DailyMed label

Azathioprine Sodium

DailyMed label · Hikma Pharmaceuticals USA Inc. · version 9

Key facts

Product Azathioprine Sodium
Labeler Hikma Pharmaceuticals USA Inc.
Document type HUMAN PRESCRIPTION DRUG LABEL
Active ingredients AZATHIOPRINE SODIUM
Active ingredient UNIIs AM94R510MS
Application number 074419
Route INTRAVENOUS
NDC package codes 0143-9566-01
Effective date Jan 23, 2025
Set ID 9ffe79a1-ac91-4a7b-a9e3-7c84bfa9ddf0

At a glance

  • 1–9 NDC package codes
  • 1–9 Active ingredients
  • None 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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