United States · FDA National Drug Code directory

Pravastatin sodium

A source-listed medicine record.

Factual source checks only. This page is not a clinically reviewed monograph. Historical or discontinued records may be included; listing does not confirm approval, current availability or pharmacy stock.

Medicine identity

Source reference
51407-889_4fffe2bf-0a75-d9a0-e063-6294a90a958f
Product NDC
51407-889
Form
TABLET
Composition / generic term
Pravastatin sodium
Labeler
Golden State Medical Supply, Inc.
Marketing category
ANDA
Marketing start / end (source format)
20180413
Source listing expiry
20271231

Source-listed ingredients

  • PRAVASTATIN SODIUM — 40 mg/1

These values do not establish equivalence or a dose recommendation.

Packages

  • 1000 TABLET in 1 BOTTLE (51407-889-10) · 51407-889-10
  • 90 TABLET in 1 BOTTLE (51407-889-90) · 51407-889-90

Source and coverage

Open FDA National Drug Code directory

Snapshot retrieved: 2026-09-17. This is the acquisition date, not a medical review date.

Clinical information, images and comparisons appear only when separately reviewed for this record. Coverage may be incomplete. Ask a pharmacist or clinician about your treatment.

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