NDC 71610-884 – Pravastatin Sodium

Pravastatin Sodium 40 mg/1 · Tablet · Oral

Human Prescription Drug

Product NDC71610-884

Product details

Brand name
Pravastatin Sodium
Generic name
Pravastatin Sodium
Labeler
Aphena Pharma Solutions - Tennessee, LLC
Dosage form
Tablet
Route
Oral
Marketing category
ANDA · ANDA209869
Marketed since
April 13, 2018
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 (3)

Package NDCDescriptionSince
71610-884-4545 TABLET in 1 BOTTLE (71610-884-45)Mar 13, 2025
71610-884-5360 TABLET in 1 BOTTLE (71610-884-53)Mar 13, 2025
71610-884-6090 TABLET in 1 BOTTLE (71610-884-60)Mar 13, 2025

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