Active Ingredient: PROCHLORPERAZINE EDISYLATE
Proprietary Name: PROCHLORPERAZINE EDISYLATE
Dosage Form; Route of Administration: CONCENTRATE; ORAL
Strength: EQ 10MG BASE/ML
Reference Listed Drug: No
Reference Standard: No
TE Code:
Application Number: A088598
Product Number: 001
Approval Date: Oct 25, 1984
Applicant Holder Full Name: MORTON GROVE PHARMACEUTICALS INC
Marketing Status:
Discontinued
Patent and Exclusivity Information