Active Ingredient: ALFENTANIL HYDROCHLORIDE
Proprietary Name: ALFENTA
Dosage Form; Route of Administration: INJECTABLE; INJECTION
Strength: EQ 0.5MG BASE/ML
Reference Listed Drug: Yes
Reference Standard: Yes
TE Code: AP
Application Number: N019353
Product Number: 001
Approval Date: Dec 29, 1986
Applicant Holder Full Name: RISING PHARMA HOLDINGS INC
Marketing Status:
Prescription
Patent and Exclusivity Information