Active Ingredient: FENTANYL CITRATE
Proprietary Name: FENTANYL CITRATE
Dosage Form; Route of Administration: INJECTABLE; INJECTION
Strength: EQ 0.05MG BASE/ML
Reference Listed Drug: No
Reference Standard: No
TE Code:
Application Number: A070637
Product Number: 001
Approval Date: Apr 30, 1990
Applicant Holder Full Name: ABBOTT LABORATORIES HOSP PRODUCTS DIV
Marketing Status:
Discontinued
Patent and Exclusivity Information