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
- 70377-048_dc0074c0-e58a-3655-2a66-084168c39615
- Product NDC
- 70377-048
- Form
- TABLET
- Composition / generic term
- Pravastatin sodium
- Labeler
- Biocon Pharma Inc.
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20210201
- Source listing expiry
- 20271231
Source-listed ingredients
- PRAVASTATIN SODIUM — 80 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 30 TABLET in 1 BOTTLE (70377-048-11) · 70377-048-11
- 90 TABLET in 1 BOTTLE (70377-048-12) · 70377-048-12
- 500 TABLET in 1 BOTTLE (70377-048-13) · 70377-048-13
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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