Active Ingredient: MICONAZOLE NITRATE
Proprietary Name: MICONAZOLE NITRATE
Dosage Form; Route of Administration: SUPPOSITORY; VAGINAL
Strength: 200MG
Reference Listed Drug: No
Reference Standard: No
TE Code: AB
Application Number: A073508
Product Number: 001
Approval Date: Nov 19, 1993
Applicant Holder Full Name: ACTAVIS PHARMA INC AN INDIRECT WHOLLY OWNED SUB OF TEVA PHARMACEUTICALS USA INC
Marketing Status:
Prescription
Patent and Exclusivity Information
