CRESTOR - 0310-0751-39 - (Rosuvastatin calcium)

Alphabetical Index


Drug Information of CRESTOR

Product NDC: 0310-0751
Proprietary Name: CRESTOR
Non Proprietary Name: Rosuvastatin calcium
Active Ingredient(s): 10    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: 0310-0751
Labeler Name: AstraZeneca Pharmaceuticals LP
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: NDA021366
Marketing Category: NDA
Start Marketing Date: 20030818

Package Information of CRESTOR

Package NDC: 0310-0751-39
Package Description: 100 TABLET, FILM COATED in 1 BOX, UNIT-DOSE (0310-0751-39)

NDC Information of CRESTOR

NDC Code 0310-0751-39
Proprietary Name CRESTOR
Package Description 100 TABLET, FILM COATED in 1 BOX, UNIT-DOSE (0310-0751-39)
Product NDC 0310-0751
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Rosuvastatin calcium
Dosage Form Name TABLET, FILM COATED
Route Name ORAL
Start Marketing Date 20030818
Marketing Category Name NDA
Labeler Name AstraZeneca Pharmaceuticals LP
Substance Name ROSUVASTATIN CALCIUM
Strength Number 10
Strength Unit mg/1
Pharmaceutical Classes HMG-CoA Reductase Inhibitor [EPC],Hydroxymethylglutaryl-CoA Reductase Inhibitors [MoA]

Complete Information of CRESTOR


General Information