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Vibativ
Vibativ - 0469-3575-50 - (telavancin hydrochloride)
Drug Information of Vibativ
| Product NDC: | 0469-3575 |
| Proprietary Name: | Vibativ |
| Non Proprietary Name: | telavancin hydrochloride |
| Active Ingredient(s): | 750 mg/1 & nbsp; telavancin hydrochloride |
| Administration Route(s): | INTRAVENOUS |
| Dosage Form(s): | INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Vibativ
| Product NDC: | 0469-3575 |
| Labeler Name: | Astellas Pharma US Inc. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | NDA022110 |
| Marketing Category: | NDA |
| Start Marketing Date: | 20091105 |
Package Information of Vibativ
| Package NDC: | 0469-3575-50 |
| Package Description: | 10 CONTAINER in 1 CARTON (0469-3575-50) > 1 INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION in 1 CONTAINER |
NDC Information of Vibativ
| NDC Code | 0469-3575-50 |
| Proprietary Name | Vibativ |
| Package Description | 10 CONTAINER in 1 CARTON (0469-3575-50) > 1 INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION in 1 CONTAINER |
| Product NDC | 0469-3575 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | telavancin hydrochloride |
| Dosage Form Name | INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION |
| Route Name | INTRAVENOUS |
| Start Marketing Date | 20091105 |
| Marketing Category Name | NDA |
| Labeler Name | Astellas Pharma US Inc. |
| Substance Name | TELAVANCIN HYDROCHLORIDE |
| Strength Number | 750 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes |
