NDC 51655-976 – Pravastatin Sodium

Pravastatin Sodium 80 mg/1 · Tablet · Oral

Human Prescription Drug

Product NDC51655-976

Product details

Brand name
Pravastatin Sodium
Generic name
Pravastatin Sodium
Labeler
Northwind Health Company, LLC
Dosage form
Tablet
Route
Oral
Marketing category
ANDA · ANDA076341
Marketed since
April 13, 2022
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 (1)

Package NDCDescriptionSince
51655-976-5230 TABLET in 1 BOTTLE, PLASTIC (51655-976-52)Apr 13, 2022

Other Pravastatin Sodium products