Atorvastatin Calcium

Product NDC

70518-0462

11-digit product format

705180462

Labeler code

70518

Product ID

70518-0462_851ed964-52d0-4bfd-e053-2a91aa0ab524

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

atorvastatin calcium

Dosage form

TABLET, FILM COATED

Route

ORAL

Labeler

REMEDYREPACK INC.

Application

ANDA091226

Marketing category

ANDA

Marketing start

2017-04-25

Marketing end

0000-00-00

Substance

ATORVASTATIN CALCIUM TRIHYDRATE

Active strength

10 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