NDC 51655-343 – Pravastatin Sodium

Pravastatin Sodium 20 mg/1 · Tablet · Oral

Human Prescription Drug

Product NDC51655-343

Product details

Brand name
Pravastatin Sodium
Generic name
Pravastatin Sodium
Labeler
Northwind Health Company, LLC
Dosage form
Tablet
Route
Oral
Marketing category
ANDA · ANDA076056
Marketed since
February 28, 2023
Marketing end
September 30, 2026
Pharmacologic class
HMG-CoA Reductase Inhibitor

Active ingredients

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

Package NDC codes (1)

Package NDCDescriptionSince
51655-343-5230 TABLET in 1 BOTTLE, PLASTIC (51655-343-52)Feb 28, 2023

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