foscarnet sodium
Rx only
Approved
Approval ID
d2b4ce68-5a81-4b14-8914-21bc38f01008
Product Type
HUMAN PRESCRIPTION DRUG LABEL
Effective Date
Jun 13, 2023
Manufacturers
FDA
Heritage Pharmaceuticals Inc. d/b/a Avet Pharmaceuticals Inc.
DUNS: 780779901
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 Code23155-771
Application NumberANDA213807
Marketing CategoryC73584
Route of AdministrationINTRAVENOUS
Effective DateJune 13, 2023
Generic Namefoscarnet sodium
INGREDIENTS (3)
FOSCARNET SODIUMActive
Quantity: 24 mg in 1 mL
Code: 964YS0OOG1
Classification: ACTIB
HYDROCHLORIC ACIDInactive
Code: QTT17582CB
Classification: IACT
WATERInactive
Code: 059QF0KO0R
Classification: IACT