Pravastatin sodium

Product NDC

68071-1917

11-digit product format

680711917

Labeler code

68071

Product ID

68071-1917_491201a8-ada6-60c4-e054-00144ff88e88

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

Pravastatin sodium

Dosage form

TABLET

Route

ORAL

Labeler

NuCare Pharmaceuticals, Inc.

Application

ANDA076939

Marketing category

ANDA

Marketing start

2006-10-23

Marketing end

0000-00-00

Substance

PRAVASTATIN SODIUM

Active strength

20 mg/1

Pharmacologic classes

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

NDC exclude flag

No

Listing certified through

2019-12-31

Current FDA listing

Historical FDA.report record