Active Ingredient: FENTANYL CITRATE
Proprietary Name: FENTANYL CITRATE
Dosage Form; Route of Administration: INJECTABLE; INJECTION
Strength: EQ 0.025MG BASE/0.5ML
Reference Listed Drug: Yes
Reference Standard: Yes
TE Code:
Application Number: N019101
Product Number: 002
Approval Date: Jan 20, 2023
Applicant Holder Full Name: HIKMA PHARMACEUTICALS USA INC
Marketing Status:
Prescription
Patent and Exclusivity Information