VANCOMYCIN HYDROCHLORIDE
Vancomycin Hydrochloride for Injection USP
Approved
Approval ID
83ea3faf-fedd-4725-911f-d71a23ec5d5e
Product Type
HUMAN PRESCRIPTION DRUG LABEL
Effective Date
Oct 11, 2019
Manufacturers
FDA
Fresenius Kabi USA, LLC
DUNS: 608775388
Products 1
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 Code63323-284
Application NumberANDA062663
Product Classification
M
Marketing Category
C73584
G
Generic Name
VANCOMYCIN HYDROCHLORIDE
Product Specifications
Route of AdministrationINTRAVENOUS
Effective DateOctober 11, 2019
FDA Product Classification
INGREDIENTS (1)
VANCOMYCIN HYDROCHLORIDEActive
Quantity: 1 g in 20 mL
Code: 71WO621TJD
Classification: ACTIM