Home
>
National Drug Code (NDC)
>
Vibativ
Vibativ - 52118-002-01 - (telavancin hydrochloride)
Drug Information of Vibativ
| Product NDC: | 52118-002 |
| Proprietary Name: | Vibativ |
| Non Proprietary Name: | telavancin hydrochloride |
| Active Ingredient(s): | 15 mg/mL & 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: | 52118-002 |
| Labeler Name: | Theravance, Inc. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | NDA022110 |
| Marketing Category: | NDA |
| Start Marketing Date: | 20091105 |
Package Information of Vibativ
| Package NDC: | 52118-002-01 |
| Package Description: | 1 VIAL, SINGLE-USE in 1 CONTAINER (52118-002-01) > 17 mL in 1 VIAL, SINGLE-USE |
NDC Information of Vibativ
| NDC Code | 52118-002-01 |
| Proprietary Name | Vibativ |
| Package Description | 1 VIAL, SINGLE-USE in 1 CONTAINER (52118-002-01) > 17 mL in 1 VIAL, SINGLE-USE |
| Product NDC | 52118-002 |
| 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 | Theravance, Inc. |
| Substance Name | TELAVANCIN HYDROCHLORIDE |
| Strength Number | 15 |
| Strength Unit | mg/mL |
| Pharmaceutical Classes |
