ATORVASTATIN CALCIUM

Product NDC

61919-916

11-digit product format

619190916

Labeler code

61919

Product ID

61919-916_5dab03d3-66b4-3311-e053-2a91aa0a0b71

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

ATORVASTATIN CALCIUM

Dosage form

TABLET, FILM COATED

Route

ORAL

Labeler

DirectRX

Application

ANDA091650

Marketing category

ANDA

Marketing start

2017-11-10

Marketing end

0000-00-00

Substance

ATORVASTATIN CALCIUM

Active strength

20 mg/1

Pharmacologic classes

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

NDC exclude flag

E

Listing certified through

2018-12-31

Current FDA listing

Historical FDA.report record