Crestor - 21695-288-90 - (Rosuvastatin calcium)

Alphabetical Index


Drug Information of Crestor

Product NDC: 21695-288
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: 21695-288
Labeler Name: Rebel Distributors Corp
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: NDA021366
Marketing Category: NDA
Start Marketing Date: 20040607

Package Information of Crestor

Package NDC: 21695-288-90
Package Description: 90 TABLET, FILM COATED in 1 BOTTLE (21695-288-90)

NDC Information of Crestor

NDC Code 21695-288-90
Proprietary Name Crestor
Package Description 90 TABLET, FILM COATED in 1 BOTTLE (21695-288-90)
Product NDC 21695-288
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Rosuvastatin calcium
Dosage Form Name TABLET, FILM COATED
Route Name ORAL
Start Marketing Date 20040607
Marketing Category Name NDA
Labeler Name Rebel Distributors Corp
Substance Name ROSUVASTATIN CALCIUM
Strength Number 20
Strength Unit mg/1
Pharmaceutical Classes

Complete Information of Crestor


General Information