Active Ingredient: MICONAZOLE NITRATE
Proprietary Name: MICONAZOLE 7 COMBINATION PACK
Dosage Form; Route of Administration: CREAM, SUPPOSITORY; TOPICAL, VAGINAL
Strength: 2%,100MG
Reference Listed Drug: No
Reference Standard: No
TE Code:
Application Number: A076585
Product Number: 001
Approval Date: Mar 26, 2004
Applicant Holder Full Name: COSETTE PHARMACEUTICALS INC
Marketing Status:
Discontinued
Patent and Exclusivity Information