Active Ingredient: PROCHLORPERAZINE EDISYLATE
Proprietary Name: PROCHLORPERAZINE
Dosage Form; Route of Administration: CONCENTRATE; ORAL
Strength: EQ 10MG BASE/ML
Reference Listed Drug: No
Reference Standard: No
TE Code:
Application Number: A087153
Product Number: 001
Approval Date: Jun 8, 1982
Applicant Holder Full Name: ALPHARMA US PHARMACEUTICALS DIVISION
Marketing Status:
Discontinued
Patent and Exclusivity Information