NDC 16729-009 – Pravastatin Sodium

Pravastatin Sodium 20 mg/1 · Tablet · Oral

Human Prescription Drug 4 recalls

Product NDC16729-009

Product details

Brand name
Pravastatin Sodium
Generic name
Pravastatin Sodium
Labeler
Accord Healthcare Inc.
Dosage form
Tablet
Route
Oral
Marketing category
ANDA · ANDA207068
Marketed since
February 16, 2017
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 (3)

Package NDCDescriptionSince
16729-009-1590 TABLET in 1 BOTTLE (16729-009-15)Feb 16, 2017
16729-009-16500 TABLET in 1 BOTTLE (16729-009-16)Feb 16, 2017
16729-009-171000 TABLET in 1 BOTTLE (16729-009-17)Feb 16, 2017

Recalls mentioning this NDC

Other Pravastatin Sodium products