Cosyntropin

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

Company

DUNS: 601458529

Effective Date

November 3, 2023

Labeling Type

HUMAN PRESCRIPTION DRUG LABEL

Active Ingredients

Tetracosactide(0.25 mg in 1 mL)

Manufacturing Establishments1

FDA-registered manufacturing facilities and establishments involved in the production, packaging, or distribution of this drug product.

Labeler

Medical Purchasing Solutions, LLC

DUNS Number

601458529

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

NDC Product Code

71872-7313

Application Number

ANDA202147

Marketing Category

ANDA (C73584)

Route of Administration

INTRAVENOUS

Effective Date

November 3, 2023

Ingredients

MANNITOLInactive

Code: 3OWL53L36AClass: IACTQuantity: 10 mg in 1 mL

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