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
- 35356-919_77f23591-e677-43b5-8ed8-47059fc8ed3f
- Product NDC
- 35356-919
- Form
- TABLET
- Composition / generic term
- pravastatin sodium
- Labeler
- Lake Erie Medical DBA Quality Care Products LLC
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20110718 / 20280430
Source-listed ingredients
- PRAVASTATIN SODIUM — 20 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 30 TABLET in 1 BOTTLE (35356-919-30) · 35356-919-30
- 90 TABLET in 1 BOTTLE (35356-919-90) · 35356-919-90
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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