Active Ingredient: AMMONIUM LACTATE
Proprietary Name: AMMONIUM LACTATE
Dosage Form; Route of Administration: CREAM; TOPICAL
Strength: EQ 12% BASE
Reference Listed Drug: No
Reference Standard: Yes
TE Code: AB
Application Number: A075774
Product Number: 001
Approval Date: May 1, 2002
Applicant Holder Full Name: PADAGIS ISRAEL PHARMACEUTICALS LTD
Marketing Status:
Prescription
Patent and Exclusivity Information
