DailyMed label

Pantoprazole Sodium

DailyMed label · State of Florida DOH Central Pharmacy · version 1

Key facts

Product Pantoprazole Sodium
Labeler State of Florida DOH Central Pharmacy
Document type HUMAN PRESCRIPTION DRUG LABEL
Active ingredients PANTOPRAZOLE SODIUM
Active ingredient UNIIs 6871619Q5X
Application number 078281
Route ORAL
NDC package codes 53808-0934-1
Effective date Mar 5, 2014
Set ID 63ef5f56-dc1b-4192-a5d8-c2d395ada656

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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