Active Ingredient: MUPIROCIN CALCIUM
Proprietary Name: MUPIROCIN
Dosage Form; Route of Administration: CREAM; TOPICAL
Strength: EQ 2% BASE
Reference Listed Drug: No
Reference Standard: Yes
TE Code: AB
Application Number: A201587
Product Number: 001
Approval Date: Jan 24, 2013
Applicant Holder Full Name: GLENMARK PHARMACEUTICALS INC USA
Marketing Status:
Prescription
Patent and Exclusivity Information
