Vancomycin Hydrochloride
Vancomycin Hydrochloride for Injection, USP(For Intravenous Use)
Approved
Approval ID
a5f2ede4-8dd0-97c6-e556-2a80f78c10c4
Product Type
HUMAN PRESCRIPTION DRUG LABEL
Effective Date
Nov 14, 2023
Manufacturers
FDA
Almaject, Inc.
DUNS: 116626205
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 Code72611-765
Application NumberANDA205694
Product Classification
M
Marketing Category
C73584
G
Generic Name
vancomycin hydrochloride
Product Specifications
Route of AdministrationINTRAVENOUS
Effective DateNovember 29, 2016
FDA Product Classification
INGREDIENTS (1)
vancomycin hydrochlorideActive
Quantity: 1 g in 20 mL
Code: 71WO621TJD
Classification: ACTIM
vancomycin hydrochloride
Product Details
FDA regulatory identification and product classification information
FDA Identifiers
NDC Product Code72611-761
Application NumberANDA205694
Product Classification
M
Marketing Category
C73584
G
Generic Name
vancomycin hydrochloride
Product Specifications
Route of AdministrationINTRAVENOUS
Effective DateNovember 29, 2016
FDA Product Classification
INGREDIENTS (1)
vancomycin hydrochlorideActive
Quantity: 500 mg in 10 mL
Code: 71WO621TJD
Classification: ACTIM