Glycophos
Glycophos
Approved
Approval ID
dcd92dc7-c6f9-4866-9edd-c95d5097c4e5
Product Type
HUMAN PRESCRIPTION DRUG LABEL
Effective Date
Dec 7, 2022
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.
SODIUM GLYCOLATE
Product Details
FDA regulatory identification and product classification information
FDA Identifiers
NDC Product Code63323-241
Product Classification
G
Generic Name
SODIUM GLYCOLATE
Product Specifications
Route of AdministrationINTRAVENOUS
Effective DateJanuary 16, 2019
FDA Product Classification
INGREDIENTS (2)
SODIUM GLYCEROPHOSPHATE ANHYDROUSActive
Quantity: 216 mg in 1 mL
Code: YP1H63LJ2K
Classification: ACTIR
HYDROCHLORIC ACIDInactive
Code: QTT17582CB
Classification: IACT