Active Ingredient: FLUCONAZOLE
Proprietary Name: FLUCONAZOLE IN SODIUM CHLORIDE 0.9% IN PLASTIC CONTAINER
Dosage Form; Route of Administration: INJECTABLE; INJECTION
Strength: 200MG/100ML (2MG/ML)
Reference Listed Drug: No
Reference Standard: No
TE Code:
Application Number: A076889
Product Number: 001
Approval Date: Mar 25, 2005
Applicant Holder Full Name: MYLAN LABORATORIES LTD
Marketing Status:
Discontinued
Patent and Exclusivity Information