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Active Ingredient: AMMONIUM LACTATE
Proprietary Name: AMMONIUM LACTATE
Dosage Form; Route of Administration: LOTION; TOPICAL
Strength: EQ 12% BASE
Reference Listed Drug: No
Reference Standard: No
TE Code: AB
Application Number: A076216
Product Number: 001
Approval Date: May 28, 2004
Applicant Holder Full Name: TARO PHARMACEUTICALS INC
Marketing Status:
Prescription
Patent and Exclusivity Information