Home
>
National Drug Code (NDC)
>
CRESTOR
CRESTOR - 52959-629-30 - (Rosuvastatin calcium)
Drug Information of CRESTOR
| Product NDC: | 52959-629 |
| 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: | 52959-629 |
| Labeler Name: | H.J. Harkins Company, Inc. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | NDA021366 |
| Marketing Category: | NDA |
| Start Marketing Date: | 20110721 |
Package Information of CRESTOR
| Package NDC: | 52959-629-30 |
| Package Description: | 30 TABLET, FILM COATED in 1 BOTTLE (52959-629-30) |
NDC Information of CRESTOR
| NDC Code | 52959-629-30 |
| Proprietary Name | CRESTOR |
| Package Description | 30 TABLET, FILM COATED in 1 BOTTLE (52959-629-30) |
| Product NDC | 52959-629 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Rosuvastatin calcium |
| Dosage Form Name | TABLET, FILM COATED |
| Route Name | ORAL |
| Start Marketing Date | 20110721 |
| Marketing Category Name | NDA |
| Labeler Name | H.J. Harkins Company, Inc. |
| Substance Name | ROSUVASTATIN CALCIUM |
| Strength Number | 20 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes | HMG-CoA Reductase Inhibitor [EPC],Hydroxymethylglutaryl-CoA Reductase Inhibitors [MoA] |
