NDC 68071-3895 – Pravastatin sodium

Pravastatin Sodium 20 mg/1 · Tablet · Oral

Human Prescription Drug

Product NDC68071-3895

Product details

Brand name
Pravastatin sodium
Generic name
Pravastatin sodium
Labeler
NuCare Pharmaceuticals, Inc.
Dosage form
Tablet
Route
Oral
Marketing category
ANDA · ANDA076056
Marketed since
February 27, 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 (1)

Package NDCDescriptionSince
68071-3895-990 TABLET in 1 BOTTLE (68071-3895-9)Sep 16, 2025

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