Cortrosyn
Cortrosyn (cosyntropin) 0.25 mg Injection, USP 1ml Vial
Approved
Approval ID
90306296-77ef-4123-9f86-8a662523cc58
Product Type
HUMAN PRESCRIPTION DRUG LABEL
Effective Date
Nov 13, 2021
Manufacturers
FDA
General Injectables & Vaccines, Inc
DUNS: 108250663
Products 1
Detailed information about drug products covered under this FDA approval, including NDC codes, dosage forms, ingredients, and administration routes.
Cortrosyn
Product Details
FDA regulatory identification and product classification information
FDA Identifiers
NDC Product Code52584-050
Application NumberNDA016750
Product Classification
M
Marketing Category
C73594
G
Generic Name
Cortrosyn
Product Specifications
Route of AdministrationPARENTERAL, INTRAVENOUS, INTRAMUSCULAR
Effective DateJuly 11, 2017
FDA Product Classification
INGREDIENTS (1)
CosyntropinActive
Quantity: 0.25 mg in 1 mL
Code: 72YY86EA29
Classification: ACTIB