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
FDA regulatory identification and product classification information
FDA Identifiers
NDC Product Code23155-771
Application NumberANDA213807
Product Classification
M
Marketing Category
C73584
G
Generic Name
foscarnet sodium
Product Specifications
Route of AdministrationINTRAVENOUS
Effective DateJune 13, 2023
FDA Product Classification
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