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Active Ingredient: PRUCALOPRIDE SUCCINATE
Proprietary Name: PRUCALOPRIDE SUCCINATE
Dosage Form; Route of Administration: TABLET; ORAL
Strength: EQ 1MG BASE
Reference Listed Drug: No
Reference Standard: No
TE Code: AB
Application Number: A218492
Product Number: 001
Approval Date: Dec 26, 2024
Applicant Holder Full Name: NOVITIUM PHARMA LLC
Marketing Status:
Prescription
Patent and Exclusivity Information
Active Ingredient: PRUCALOPRIDE SUCCINATE
Proprietary Name: PRUCALOPRIDE SUCCINATE
Dosage Form; Route of Administration: TABLET; ORAL
Strength: EQ 2MG BASE
Reference Listed Drug: No
Reference Standard: No
TE Code: AB
Application Number: A218492
Product Number: 002
Approval Date: Dec 26, 2024
Applicant Holder Full Name: NOVITIUM PHARMA LLC
Marketing Status:
Prescription
Patent and Exclusivity Information