NDC 71205-149 – Pravastatin Sodium

Pravastatin Sodium 20 mg/1 · Tablet · Oral

Human Prescription Drug

Product NDC71205-149

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
71205-149-3030 TABLET in 1 BOTTLE (71205-149-30)Nov 1, 2018
71205-149-6060 TABLET in 1 BOTTLE (71205-149-60)Nov 1, 2018
71205-149-9090 TABLET in 1 BOTTLE (71205-149-90)Nov 1, 2018

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