NDC 16714-570 – Pravastatin Sodium

Pravastatin Sodium 80 mg/1 · Tablet · Oral

Human Prescription Drug 2 recalls

Product NDC16714-570

Product details

Brand name
Pravastatin Sodium
Generic name
Pravastatin Sodium
Labeler
NorthStar RxLLC
Dosage form
Tablet
Route
Oral
Marketing category
ANDA · ANDA077987
Marketed since
August 12, 2022
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 (2)

Package NDCDescriptionSince
16714-570-0190 TABLET in 1 BOTTLE (16714-570-01)Aug 12, 2022
16714-570-02500 TABLET in 1 BOTTLE (16714-570-02)Aug 12, 2022

Recalls mentioning this NDC

Other Pravastatin Sodium products