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Crestor
Crestor - 35356-413-30 - (Rosuvastatin calcium)
Drug Information of Crestor
| Product NDC: | 35356-413 |
| Proprietary Name: | Crestor |
| Non Proprietary Name: | Rosuvastatin calcium |
| Active Ingredient(s): | 40 mg/1 & nbsp; Rosuvastatin calcium |
| Administration Route(s): | ORAL |
| Dosage Form(s): | TABLET, COATED |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Crestor
| Product NDC: | 35356-413 |
| Labeler Name: | Lake Erie Medical DBA Quality Care Products LLC |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | NDA021366 |
| Marketing Category: | NDA |
| Start Marketing Date: | 20100908 |
Package Information of Crestor
| Package NDC: | 35356-413-30 |
| Package Description: | 30 TABLET, COATED in 1 BOTTLE, PLASTIC (35356-413-30) |
NDC Information of Crestor
| NDC Code | 35356-413-30 |
| Proprietary Name | Crestor |
| Package Description | 30 TABLET, COATED in 1 BOTTLE, PLASTIC (35356-413-30) |
| Product NDC | 35356-413 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Rosuvastatin calcium |
| Dosage Form Name | TABLET, COATED |
| Route Name | ORAL |
| Start Marketing Date | 20100908 |
| Marketing Category Name | NDA |
| Labeler Name | Lake Erie Medical DBA Quality Care Products LLC |
| Substance Name | ROSUVASTATIN CALCIUM |
| Strength Number | 40 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes |
