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: A089903
Product Number: 001
Approval Date: Aug 29, 1989
Applicant Holder Full Name: HIKMA PHARMACEUTICALS USA INC
Marketing Status:
Prescription
Patent and Exclusivity Information