NDC 71610-879 – Pravastatin Sodium

Pravastatin Sodium 40 mg/1 · Tablet · Oral

Human Prescription Drug

Product NDC71610-879

Product details

Brand name
Pravastatin Sodium
Generic name
Pravastatin Sodium
Labeler
Aphena Pharma Solutions - Tennessee, LLC
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 (3)

Package NDCDescriptionSince
71610-879-4545 TABLET in 1 BOTTLE (71610-879-45)Feb 13, 2025
71610-879-5360 TABLET in 1 BOTTLE (71610-879-53)Feb 13, 2025
71610-879-6090 TABLET in 1 BOTTLE (71610-879-60)Feb 13, 2025

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