Active Ingredient: FLUCONAZOLE
Proprietary Name: FLUCONAZOLE IN SODIUM CHLORIDE 0.9%
Dosage Form; Route of Administration: INJECTABLE; INJECTION
Strength: 200MG/100ML (2MG/ML)
Reference Listed Drug: No
Reference Standard: No
TE Code: AP
Application Number: A076145
Product Number: 001
Approval Date: Jul 29, 2004
Applicant Holder Full Name: FRESENIUS KABI USA LLC
Marketing Status:
Prescription
Patent and Exclusivity Information