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
- 68788-7660_418c65fd-0357-4974-87ae-7246a23b87cb
- Product NDC
- 68788-7660
- Form
- TABLET
- Composition / generic term
- PRAVASTATIN SODIUM
- Labeler
- Preferred Pharmaceuticals Inc..
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20220927
- Source listing expiry
- 20271231
Source-listed ingredients
- PRAVASTATIN SODIUM — 80 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 100 TABLET in 1 BOTTLE (68788-7660-0) · 68788-7660-0
- 20 TABLET in 1 BOTTLE (68788-7660-2) · 68788-7660-2
- 30 TABLET in 1 BOTTLE (68788-7660-3) · 68788-7660-3
- 60 TABLET in 1 BOTTLE (68788-7660-6) · 68788-7660-6
- 120 TABLET in 1 BOTTLE (68788-7660-8) · 68788-7660-8
- 90 TABLET in 1 BOTTLE (68788-7660-9) · 68788-7660-9
Source and coverage
Open FDA National Drug Code directory →
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.
Browse United States records →