ATORVASTATIN CALCIUM

Product NDC

68645-483

11-digit product format

686450483

Labeler code

68645

Product ID

68645-483_fa2859b2-d351-4c9c-ad0b-eec6b493ff9f

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

ATORVASTATIN CALCIUM

Dosage form

TABLET, FILM COATED

Route

ORAL

Labeler

Legacy Pharmaceutical Packaging, LLC

Application

NDA020702

Marketing category

NDA AUTHORIZED GENERIC

Marketing start

2011-11-30

Marketing end

2020-08-31

Substance

ATORVASTATIN CALCIUM TRIHYDRATE

Active strength

40 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