PRAVASTATIN SODIUM

Product NDC

68788-7253

11-digit product format

687887253

Labeler code

68788

Product ID

68788-7253_c8252719-b2d5-46ab-9ba1-5cadfad13013

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

PRAVASTATIN SODIUM

Dosage form

TABLET

Route

ORAL

Labeler

Preferred Pharmaceuticals Inc.

Application

ANDA207068

Marketing category

ANDA

Marketing start

2018-09-11

Marketing end

0000-00-00

Substance

PRAVASTATIN SODIUM

Active strength

40 mg/1

Pharmacologic classes

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

NDC exclude flag

No

Listing certified through

2020-12-31

Current FDA listing

Historical FDA.report record