NDC 60687-897 – Pravastatin Sodium

Pravastatin Sodium 20 mg/1 · Tablet · Oral

Human Prescription Drug

Product NDC60687-897

Product details

Brand name
Pravastatin Sodium
Generic name
Pravastatin Sodium
Labeler
American Health Packaging
Dosage form
Tablet
Route
Oral
Marketing category
ANDA · ANDA077987
Marketed since
March 2, 2025
Marketing end
April 30, 2027
Pharmacologic class
HMG-CoA Reductase Inhibitor

Active ingredients

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

Package NDC codes (1)

Package NDCDescriptionSince
60687-897-01100 BLISTER PACK in 1 CARTON (60687-897-01) / 1 TABLET in 1 BLISTER PACK (60687-897-11)Mar 2, 2025

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