NDC 68788-4049 – Pravastatin sodium

Pravastatin Sodium 20 mg/1 · Tablet · Oral

Human Prescription Drug

Product NDC68788-4049

Product details

Brand name
Pravastatin sodium
Generic name
Pravastatin sodium
Labeler
Preferred Pharmaceuticals Inc.
Dosage form
Tablet
Route
Oral
Marketing category
ANDA · ANDA076056
Marketed since
October 31, 2025
Listing expires
December 31, 2026
Pharmacologic class
HMG-CoA Reductase Inhibitor

Active ingredients

Uses, dosage, side effects and warnings for Pravastatin Sodium →

Package NDC codes (3)

Package NDCDescriptionSince
68788-4049-330 TABLET in 1 BOTTLE (68788-4049-3)Oct 31, 2025
68788-4049-660 TABLET in 1 BOTTLE (68788-4049-6)Oct 31, 2025
68788-4049-990 TABLET in 1 BOTTLE (68788-4049-9)Oct 31, 2025

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