ATORVASTATIN CALCIUM

Product NDC

0179-0141

11-digit product format

001790141

Labeler code

0179

Product ID

0179-0141_7b9692cd-41f1-0806-e053-2991aa0a74f6

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

ATORVASTATIN CALCIUM

Dosage form

TABLET, FILM COATED

Route

ORAL

Labeler

KAISER FOUNDATION HOSPITALS

Application

NDA020702

Marketing category

NDA AUTHORIZED GENERIC

Marketing start

2013-11-05

Marketing end

2020-07-31

Substance

ATORVASTATIN CALCIUM TRIHYDRATE

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