NDC 71205-516 – Pravastatin Sodium

Pravastatin Sodium 40 mg/1 · Tablet · Oral

Human Prescription Drug

Product NDC71205-516

Product details

Brand name
Pravastatin Sodium
Generic name
Pravastatin Sodium
Labeler
Proficient Rx LP
Dosage form
Tablet
Route
Oral
Marketing category
ANDA · ANDA076341
Marketed since
July 18, 2011
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
71205-516-3030 TABLET in 1 BOTTLE (71205-516-30)Dec 24, 2020
71205-516-6060 TABLET in 1 BOTTLE (71205-516-60)Dec 24, 2020
71205-516-9090 TABLET in 1 BOTTLE (71205-516-90)Dec 24, 2020

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