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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: A203918
Product Number: 001
Approval Date: Jun 15, 2016
Applicant Holder Full Name: PAR PHARMACEUTICAL INC
Marketing Status:
Prescription
Patent and Exclusivity Information
