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
- 82009-007_a8435e8a-3fa3-1d2d-bd06-ed67cc63bd7a
- Product NDC
- 82009-007
- Form
- TABLET
- Composition / generic term
- PRAVASTATIN SODIUM
- Labeler
- Quallent
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20211203
- 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 (82009-007-10) · 82009-007-10
- 90 TABLET in 1 BOTTLE (82009-007-90) · 82009-007-90
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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