Cortrosyn

FDA-approved pharmaceutical product with comprehensive regulatory information, manufacturing details, and complete labeling documentation.

Company

DUNS: 108250663

Effective Date

November 13, 2021

Labeling Type

HUMAN PRESCRIPTION DRUG LABEL

Active Ingredients

Tetracosactide(0.25 mg in 1 mL)

Products1

Detailed information about drug products covered under this FDA approval, including NDC codes, dosage forms, ingredients, and administration routes.

NDC Product Code

52584-050

Application Number

NDA016750

Marketing Category

NDA (C73594)

Route of Administration

PARENTERAL, INTRAVENOUS, INTRAMUSCULAR

Effective Date

July 11, 2017

Ingredients

Code: 72YY86EA29Class: ACTIBQuantity: 0.25 mg in 1 mL