Rosuvastatin Calcium

Product NDC

0093-7572

11-digit product format

000937572

Labeler code

0093

Product ID

0093-7572_83cfa277-158e-466a-8fcf-703495f858f7

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

Rosuvastatin Calcium

Dosage form

TABLET, FILM COATED

Route

ORAL

Labeler

Teva Pharmaceuticals USA, Inc.

Application

ANDA079166

Marketing category

ANDA

Marketing start

2016-08-18

Marketing end

2019-10-31

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

0000-00-00

Current FDA listing

Historical FDA.report record