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:
Application Number: A089530
Product Number: 001
Approval Date: Jul 8, 1987
Applicant Holder Full Name: WATSON LABORATORIES INC
Marketing Status:
Discontinued
Patent and Exclusivity Information
