Pravastatin Sodium

Product NDC

70518-0304

11-digit product format

705180304

Labeler code

70518

Product ID

70518-0304_a131d099-8b94-566b-e053-2a95a90a45b9

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

Pravastatin Sodium

Dosage form

TABLET

Route

ORAL

Labeler

REMEDYREPACK INC.

Application

ANDA077987

Marketing category

ANDA

Marketing start

2017-03-10

Marketing end

0000-00-00

Substance

PRAVASTATIN SODIUM

Active strength

80 mg/1

Pharmacologic classes

HMG-CoA Reductase Inhibitor [EPC],Hydroxymethylglutaryl-CoA Reductase Inhibitors [MoA]

NDC exclude flag

No

Listing certified through

2021-12-31

Current FDA listing

Historical FDA.report record