NDC 68788-7660 – Pravastatin Sodium

Pravastatin Sodium 80 mg/1 · Tablet · Oral

Human Prescription Drug

Product NDC68788-7660

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 (6)

Package NDCDescriptionSince
68788-7660-0100 TABLET in 1 BOTTLE (68788-7660-0)Sep 27, 2022
68788-7660-220 TABLET in 1 BOTTLE (68788-7660-2)Sep 27, 2022
68788-7660-330 TABLET in 1 BOTTLE (68788-7660-3)Sep 27, 2022
68788-7660-660 TABLET in 1 BOTTLE (68788-7660-6)Sep 27, 2022
68788-7660-8120 TABLET in 1 BOTTLE (68788-7660-8)Sep 27, 2022
68788-7660-990 TABLET in 1 BOTTLE (68788-7660-9)Sep 27, 2022

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