DailyMed label

Alendronate Sodium

DailyMed label · Aidarex Pharmaceuticals LLC · version 1

Key facts

Product Alendronate Sodium
Labeler Aidarex Pharmaceuticals LLC
Document type HUMAN PRESCRIPTION DRUG LABEL
Active ingredients ALENDRONATE SODIUM
Active ingredient UNIIs 2UY4M2U3RA
Application number 075710
Route ORAL
NDC package codes 33261-993-01
Effective date Nov 14, 2013
Set ID f3840bb8-f1aa-4d20-bca1-c0b986e40f22

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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