Vancomycin Hydrochloride
Vancomycin Hydrochloride for Injection, USP
Approved
Approval ID
f28e3c2b-ae31-4c2a-8178-53962b7b213c
Product Type
HUMAN PRESCRIPTION DRUG LABEL
Effective Date
Sep 22, 2022
Manufacturers
FDA
BluePoint Laboratories
DUNS: 985523874
Products 2
Detailed information about drug products covered under this FDA approval, including NDC codes, dosage forms, ingredients, and administration routes.
Vancomycin Hydrochloride
Product Details
FDA regulatory identification and product classification information
FDA Identifiers
NDC Product Code68001-406
Application NumberANDA204125
Product Classification
M
Marketing Category
C73584
G
Generic Name
Vancomycin Hydrochloride
Product Specifications
Route of AdministrationINTRAVENOUS
Effective DateSeptember 22, 2022
FDA Product Classification
INGREDIENTS (1)
VANCOMYCIN HYDROCHLORIDEActive
Quantity: 5 g in 1 1
Code: 71WO621TJD
Classification: ACTIM
Vancomycin Hydrochloride
Product Details
FDA regulatory identification and product classification information
FDA Identifiers
NDC Product Code68001-407
Application NumberANDA204125
Product Classification
M
Marketing Category
C73584
G
Generic Name
Vancomycin Hydrochloride
Product Specifications
Route of AdministrationINTRAVENOUS
Effective DateSeptember 22, 2022
FDA Product Classification
INGREDIENTS (1)
VANCOMYCIN HYDROCHLORIDEActive
Quantity: 10 g in 1 1
Code: 71WO621TJD
Classification: ACTIM