Active Ingredient: SODIUM PHENYLBUTYRATE
Proprietary Name: SODIUM PHENYLBUTYRATE
Dosage Form; Route of Administration: POWDER; ORAL
Strength: 3GM/TEASPOONFUL
Reference Listed Drug: No
Reference Standard: No
TE Code: AB
Application Number: A202819
Product Number: 001
Approval Date: Mar 22, 2013
Applicant Holder Full Name: SIGMAPHARM LABORATORIES LLC
Marketing Status:
Prescription
Patent and Exclusivity Information
