Active Ingredient: MUPIROCIN CALCIUM
Proprietary Name: MUPIROCIN
Dosage Form; Route of Administration: CREAM; TOPICAL
Strength: EQ 2% BASE
Reference Listed Drug: No
Reference Standard: No
TE Code: AB
Application Number: A213053
Product Number: 001
Approval Date: Nov 16, 2021
Applicant Holder Full Name: ALEMBIC PHARMACEUTICALS LTD
Marketing Status:
Prescription
Patent and Exclusivity Information
