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
NDC Product Code63323-875
Application NumberANDA212483
Marketing CategoryC73584
Route of AdministrationINTRAVENOUS
Effective DateJanuary 29, 2021
Generic Namefoscarnet sodium
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