NDC 82009-006 – Pravastatin Sodium

Pravastatin Sodium 20 mg/1 · Tablet · Oral

Human Prescription Drug

Product NDC82009-006

Product details

Brand name
Pravastatin Sodium
Generic name
Pravastatin Sodium
Labeler
Quallent
Dosage form
Tablet
Route
Oral
Marketing category
ANDA · ANDA076341
Marketed since
December 3, 2021
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 (1)

Package NDCDescriptionSince
82009-006-101000 TABLET in 1 BOTTLE (82009-006-10)Dec 3, 2021

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