NDC 66220-315

VIBATIV

Telavancin Hydrochloride

VIBATIV is a Intravenous Injection, Powder, Lyophilized, For Solution in the Human Prescription Drug category. It is labeled and distributed by Cumberland Pharmaceuticals Inc.. The primary component is Telavancin Hydrochloride.

Product ID66220-315_ed26baa1-fb7b-485e-b53f-74694de6c086
NDC66220-315
Product TypeHuman Prescription Drug
Proprietary NameVIBATIV
Generic NameTelavancin Hydrochloride
Dosage FormInjection, Powder, Lyophilized, For Solution
Route of AdministrationINTRAVENOUS
Marketing Start Date2021-01-01
Marketing CategoryNDA / NDA
Application NumberNDA022110
Labeler NameCumberland Pharmaceuticals Inc.
Substance NameTELAVANCIN HYDROCHLORIDE
Active Ingredient Strength15 mg/mg
Pharm ClassesLipoglycopeptide Antibacterial [EPC],Lipoglycopeptides [EXT]
NDC Exclude FlagN
Listing Certified Through2022-12-31

Packaging

NDC 66220-315-11

1 VIAL in 1 CARTON (66220-315-11) > 15 mg in 1 VIAL
Marketing Start Date2021-01-01
NDC Exclude FlagN
Sample Package?N

Drug Details

NDC Crossover Matching brand name "VIBATIV" or generic name "Telavancin Hydrochloride"

NDCBrand NameGeneric Name
52118-001Vibativtelavancin hydrochloride
52118-002Vibativtelavancin hydrochloride
62847-001Vibativtelavancin hydrochloride
62847-002Vibativtelavancin hydrochloride
66220-315VIBATIVtelavancin hydrochloride

Trademark Results [VIBATIV]

Mark Image

Registration | Serial
Company
Trademark
Application Date
VIBATIV
VIBATIV
79035545 3939879 Live/Registered
Cumberland Pharmaceuticals Inc.
2007-01-22

© 2024 FDA.report
This site is not affiliated with or endorsed by the FDA.