CRESTOR - 55154-6924-9 - (Rosuvastatin calcium)

Alphabetical Index


Drug Information of CRESTOR

Product NDC: 55154-6924
Proprietary Name: CRESTOR
Non Proprietary Name: Rosuvastatin calcium
Active Ingredient(s): 20    mg/1 & nbsp;   Rosuvastatin calcium
Administration Route(s): ORAL
Dosage Form(s): TABLET, FILM COATED
Coding System: National Drug Codes(NDC)

Labeler Information of CRESTOR

Product NDC: 55154-6924
Labeler Name: Cardinal Health
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: NDA021366
Marketing Category: NDA
Start Marketing Date: 20101201

Package Information of CRESTOR

Package NDC: 55154-6924-9
Package Description: 2520 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (55154-6924-9)

NDC Information of CRESTOR

NDC Code 55154-6924-9
Proprietary Name CRESTOR
Package Description 2520 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (55154-6924-9)
Product NDC 55154-6924
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Rosuvastatin calcium
Dosage Form Name TABLET, FILM COATED
Route Name ORAL
Start Marketing Date 20101201
Marketing Category Name NDA
Labeler Name Cardinal Health
Substance Name ROSUVASTATIN CALCIUM
Strength Number 20
Strength Unit mg/1
Pharmaceutical Classes

Complete Information of CRESTOR


General Information