Anticoagulant Sodium Citrate
Anticoagulant Sodium Citrate Solution, USPCode 798-60
Approved
Approval ID
3a8dfcfa-e034-40ca-a71f-05099015f87d
Product Type
HUMAN PRESCRIPTION DRUG LABEL
Effective Date
May 20, 2011
Manufacturers
FDA
Medsep Corporation
DUNS: 928224765
Products 1
Detailed information about drug products covered under this FDA approval, including NDC codes, dosage forms, ingredients, and administration routes.
Sodium Citrate
Product Details
FDA regulatory identification and product classification information
FDA Identifiers
NDC Product Code62646-798
Application NumberNDA760305
Product Classification
M
Marketing Category
C73594
G
Generic Name
Sodium Citrate
Product Specifications
Route of AdministrationINTRAVENOUS
Effective DateMay 20, 2011
FDA Product Classification
INGREDIENTS (2)
WATERInactive
Code: 059QF0KO0R
Classification: IACT
SODIUM CITRATEActive
Quantity: 10 g in 250 mL
Code: 1Q73Q2JULR
Classification: ACTIB