Active Ingredient: PROCHLORPERAZINE EDISYLATE
Proprietary Name: PROCHLORPERAZINE EDISYLATE
Dosage Form; Route of Administration: INJECTABLE; INJECTION
Strength: EQ 5MG BASE/ML
Reference Listed Drug: No
Reference Standard: No
TE Code: AP
Application Number: A213873
Product Number: 001
Approval Date: Jul 14, 2022
Applicant Holder Full Name: EUGIA PHARMA SPECIALITIES LTD
Marketing Status:
Prescription
Patent and Exclusivity Information