DailyMed label

Pravastatin sodium

DailyMed label · Dr.Reddy's Laboratories Limited · version 7

Key facts

Product Pravastatin sodium
Labeler Dr.Reddy's Laboratories Limited
Document type HUMAN PRESCRIPTION DRUG LABEL
Active ingredients PRAVASTATIN SODIUM
Active ingredient UNIIs 3M8608UQ61
Application number 076714
Route ORAL
NDC package codes 55111-229-30, 55111-229-90, 55111-229-01, 55111-229-05, 55111-230-30, 55111-230-90, 55111-230-01, 55111-230-05, 55111-231-30, 55111-231-90, 55111-231-01, 55111-231-05 and 4 more
Effective date Nov 21, 2018
Set ID 99cc0546-bb2d-751e-edfd-1c15a1182e0c

At a glance

  • 10–99 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.

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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