NDC 68788-7779 – Pravastatin Sodium

Pravastatin Sodium 20 mg/1 · Tablet · Oral

Human Prescription Drug

Product NDC68788-7779

Product details

Brand name
Pravastatin Sodium
Generic name
Pravastatin Sodium
Labeler
Preferred Pharmaceuticals Inc.
Dosage form
Tablet
Route
Oral
Marketing category
ANDA · ANDA076341
Marketed since
September 27, 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 (3)

Package NDCDescriptionSince
68788-7779-390 TABLET in 1 BOTTLE (68788-7779-3)Sep 27, 2022
68788-7779-6100 TABLET in 1 BOTTLE (68788-7779-6)Sep 27, 2022
68788-7779-9500 TABLET in 1 BOTTLE (68788-7779-9)Sep 27, 2022

Other Pravastatin Sodium products