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
- 0904-5892_1fc88a70-8c13-4db5-97e5-e0f356ce65aa
- Product NDC
- 0904-5892
- Form
- TABLET
- Composition / generic term
- PRAVASTATIN SODIUM
- Labeler
- Major Pharmaceuticals
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20110718
- Source listing expiry
- 20271231
Source-listed ingredients
- PRAVASTATIN SODIUM — 20 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 100 BLISTER PACK in 1 BOX, UNIT-DOSE (0904-5892-61) / 1 TABLET in 1 BLISTER PACK · 0904-5892-61
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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