DailyMed label

pravastatin sodium

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

Key facts

Product pravastatin sodium
Labeler State of Florida DOH Central Pharmacy
Document type HUMAN PRESCRIPTION DRUG LABEL
Active ingredients PRAVASTATIN SODIUM
Active ingredient UNIIs 3M8608UQ61
Application number 077751
Route ORAL
NDC package codes 53808-0874-2, 53808-0875-2
Effective date Sep 27, 2013
Set ID 5318e92a-aa98-4890-870e-e4dec3f6069e

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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