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: 69292-101_52351ef8-7a5a-6e07-e063-6294a90af72a
Product NDC: 69292-101
Form: TABLET
Composition / generic term: Pravastatin Sodium
Labeler: Amici Pharma, Inc.
Marketing category: ANDA
Marketing start / end (source format): 20260519
Source listing expiry: 20271231

Source-listed ingredients

PRAVASTATIN SODIUM — 10 mg/1

These values do not establish equivalence or a dose recommendation.

Packages

1000 TABLET in 1 BOTTLE (69292-101-10) · 69292-101-10
500 TABLET in 1 BOTTLE (69292-101-50) · 69292-101-50
90 TABLET in 1 BOTTLE (69292-101-90) · 69292-101-90

Source and coverage

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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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