PRAVACHOL

Product NDC

0003-5195

11-digit product format

000035195

Labeler code

0003

Product ID

0003-5195_e295e36d-f5f2-49e6-acef-ecd9d029a6d3

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

PRAVASTATIN SODIUM

Dosage form

TABLET

Route

ORAL

Labeler

E.R. Squibb & Sons, L.L.C.

Application

NDA019898

Marketing category

NDA

Marketing start

2009-06-01

Marketing end

2020-03-31

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

0000-00-00

Current FDA listing

Historical FDA.report record