Vibativ - 52118-002-01 - (telavancin hydrochloride)

Alphabetical Index


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

Complete Information of Vibativ


General Information