Rosuvastatin Calcium

Product NDC

70518-0167

11-digit product format

705180167

Labeler code

70518

Product ID

70518-0167_5d1e7505-4dca-54dc-e053-2991aa0aab1d

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

Rosuvastatin calcium

Dosage form

TABLET

Route

ORAL

Labeler

REMEDYREPACK INC.

Application

ANDA079167

Marketing category

ANDA

Marketing start

2017-02-01

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

E

Listing certified through

2018-12-31

Current FDA listing

Historical FDA.report record