NDC 71335-0692 – Pravastatin Sodium

Pravastatin Sodium 40 mg/1 · Tablet · Oral

Human Prescription Drug

Product NDC71335-0692

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, 2027
Pharmacologic class
HMG-CoA Reductase Inhibitor

Active ingredients

Uses, dosage, side effects and warnings for Pravastatin Sodium →

Package NDC codes (5)

Package NDCDescriptionSince
71335-0692-130 TABLET in 1 BOTTLE (71335-0692-1)May 4, 2018
71335-0692-260 TABLET in 1 BOTTLE (71335-0692-2)Jul 31, 2019
71335-0692-390 TABLET in 1 BOTTLE (71335-0692-3)Feb 14, 2018
71335-0692-4100 TABLET in 1 BOTTLE (71335-0692-4)Jan 29, 2025
71335-0692-510 TABLET in 1 BOTTLE (71335-0692-5)Jan 29, 2025

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