pravastatin sodium

Product NDC

70518-0707

11-digit product format

705180707

Labeler code

70518

Product ID

70518-0707_8b4f8d3f-8110-fa40-e053-2a95a90a12d6

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

pravastatin sodium

Dosage form

TABLET

Route

ORAL

Labeler

REMEDYREPACK INC.

Application

ANDA077751

Marketing category

ANDA

Marketing start

2017-08-22

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

2020-12-31

Current FDA listing

Historical FDA.report record