NDC 0093-7202 – Pravastatin Sodium

Pravastatin Sodium 40 mg/1 · Tablet · Oral

Human Prescription Drug

Product NDC0093-7202

Product details

Brand name
Pravastatin Sodium
Generic name
Pravastatin Sodium
Labeler
Teva Pharmaceuticals USA, Inc.
Dosage form
Tablet
Route
Oral
Marketing category
ANDA · ANDA076056
Marketed since
April 25, 2006
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 (2)

Package NDCDescriptionSince
0093-7202-101000 TABLET in 1 BOTTLE (0093-7202-10)Apr 25, 2006
0093-7202-9890 TABLET in 1 BOTTLE (0093-7202-98)Apr 25, 2006

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