DailyMed label

Pravastatin Sodium

DailyMed label · Teva Pharmaceuticals USA, Inc. · version 27

Key facts

Product Pravastatin Sodium
Labeler Teva Pharmaceuticals USA, Inc.
Document type HUMAN PRESCRIPTION DRUG LABEL
Active ingredients PRAVASTATIN SODIUM
Active ingredient UNIIs 3M8608UQ61
Application number 076056
Route ORAL
NDC package codes 0093-0771-98, 0093-0771-10, 0093-7201-98, 0093-7201-10, 0093-7202-98, 0093-7202-10
Effective date Jan 1, 2024
Set ID 99e0e848-f8f3-4b42-b880-8fbc42633948

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.

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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