Cosyntropin
cosyntropin for injection For diagnostic use only
Approved
Approval ID
09441f78-7350-0cb3-e063-6394a90a46ab
Product Type
HUMAN PRESCRIPTION DRUG LABEL
Effective Date
Nov 3, 2023
Manufacturers
FDA
Medical Purchasing Solutions, LLC
DUNS: 601458529
Products 1
Detailed information about drug products covered under this FDA approval, including NDC codes, dosage forms, ingredients, and administration routes.
Cosyntropin
Product Details
FDA regulatory identification and product classification information
FDA Identifiers
NDC Product Code71872-7313
Application NumberANDA202147
Product Classification
M
Marketing Category
C73584
G
Generic Name
Cosyntropin
Product Specifications
Route of AdministrationINTRAVENOUS
Effective DateNovember 3, 2023
FDA Product Classification
INGREDIENTS (2)
MANNITOLInactive
Quantity: 10 mg in 1 mL
Code: 3OWL53L36A
Classification: IACT
COSYNTROPINActive
Quantity: 0.25 mg in 1 mL
Code: 72YY86EA29
Classification: ACTIB