Fentanyl Citrate

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

Company

Cantrell Drug Company

DUNS: 035545763

Effective Date

May 15, 2013

Labeling Type

HUMAN PRESCRIPTION DRUG LABEL

Active Ingredients

Fentanyl(20 ug 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

52533-025

Route of Administration

INTRAVENOUS

Effective Date

January 30, 2013

Ingredients

Code: MUN5LYG46HClass: ACTIMQuantity: 20 ug in 1 mL

Sodium ChlorideInactive

Code: 451W47IQ8XClass: IACTQuantity: 9 mg in 1 mL

WaterInactive

Code: 059QF0KO0RClass: IACT