Rosuvastatin calcium

Product NDC

70518-1745

11-digit product format

705181745

Labeler code

70518

Product ID

70518-1745_967db213-201a-5529-e053-2a95a90a1dbb

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

Rosuvastatin Calcium

Dosage form

TABLET, FILM COATED

Route

ORAL

Labeler

REMEDYREPACK INC.

Application

ANDA207752

Marketing category

ANDA

Marketing start

2018-12-20

Marketing end

0000-00-00

Substance

ROSUVASTATIN CALCIUM

Active strength

20 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