Foscarnet
Approved
Approval ID
335f7deb-a045-43cb-b319-d7b73bfda73c
Product Type
HUMAN PRESCRIPTION DRUG LABEL
Effective Date
Jun 9, 2021
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.
foscarnet sodium
Product Details
FDA regulatory identification and product classification information
FDA Identifiers
NDC Product Code63323-875
Application NumberANDA212483
Product Classification
M
Marketing Category
C73584
G
Generic Name
foscarnet sodium
Product Specifications
Route of AdministrationINTRAVENOUS
Effective DateJanuary 29, 2021
FDA Product Classification
INGREDIENTS (3)
hydrochloric acidInactive
Code: QTT17582CB
Classification: IACT
foscarnet sodiumActive
Quantity: 24 mg in 1 mL
Code: 964YS0OOG1
Classification: ACTIB
waterInactive
Code: 059QF0KO0R
Classification: IACT