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