NDC 63629-7508 – Pravastatin Sodium

Pravastatin Sodium 80 mg/1 · Tablet · Oral

Human Prescription Drug

Product NDC63629-7508

Product details

Brand name
Pravastatin Sodium
Generic name
Pravastatin Sodium
Labeler
Bryant Ranch Prepack
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 (5)

Package NDCDescriptionSince
63629-7508-130 TABLET in 1 BOTTLE (63629-7508-1)Jan 8, 2019
63629-7508-290 TABLET in 1 BOTTLE (63629-7508-2)Jan 19, 2018
63629-7508-358 TABLET in 1 BOTTLE (63629-7508-3)Mar 19, 2021
63629-7508-488 TABLET in 1 BOTTLE (63629-7508-4)Mar 26, 2021
63629-7508-510 TABLET in 1 BOTTLE (63629-7508-5)Jan 24, 2025

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