NDC 68071-3361 – Pravastatin Sodium

Pravastatin Sodium 20 mg/1 · Tablet · Oral

Human Prescription Drug

Product NDC68071-3361

Product details

Brand name
Pravastatin Sodium
Generic name
Pravastatin Sodium
Labeler
NuCare Pharmaceuticals, Inc.
Dosage form
Tablet
Route
Oral
Marketing category
ANDA · ANDA076341
Marketed since
July 18, 2011
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 (2)

Package NDCDescriptionSince
68071-3361-330 TABLET in 1 BOTTLE (68071-3361-3)Jul 12, 2017
68071-3361-990 TABLET in 1 BOTTLE (68071-3361-9)Jul 12, 2017

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