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Teflaro
Teflaro - 0456-0600-10 - (ceftaroline fosamil)
Drug Information of Teflaro
| Product NDC: | 0456-0600 |
| Proprietary Name: | Teflaro |
| Non Proprietary Name: | ceftaroline fosamil |
| Active Ingredient(s): | 600 mg/20mL & nbsp; ceftaroline fosamil |
| Administration Route(s): | INTRAVENOUS |
| Dosage Form(s): | POWDER, FOR SOLUTION |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Teflaro
| Product NDC: | 0456-0600 |
| Labeler Name: | Forest Laboratories, Inc. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | NDA200327 |
| Marketing Category: | NDA |
| Start Marketing Date: | 20101029 |
Package Information of Teflaro
| Package NDC: | 0456-0600-10 |
| Package Description: | 10 VIAL, SINGLE-DOSE in 1 CARTON (0456-0600-10) > 20 mL in 1 VIAL, SINGLE-DOSE (0456-0600-01) |
NDC Information of Teflaro
| NDC Code | 0456-0600-10 |
| Proprietary Name | Teflaro |
| Package Description | 10 VIAL, SINGLE-DOSE in 1 CARTON (0456-0600-10) > 20 mL in 1 VIAL, SINGLE-DOSE (0456-0600-01) |
| Product NDC | 0456-0600 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | ceftaroline fosamil |
| Dosage Form Name | POWDER, FOR SOLUTION |
| Route Name | INTRAVENOUS |
| Start Marketing Date | 20101029 |
| Marketing Category Name | NDA |
| Labeler Name | Forest Laboratories, Inc. |
| Substance Name | CEFTAROLINE FOSAMIL |
| Strength Number | 600 |
| Strength Unit | mg/20mL |
| Pharmaceutical Classes |
