Active Ingredient: PROCHLORPERAZINE MALEATE
Proprietary Name: PROCHLORPERAZINE MALEATE
Dosage Form; Route of Administration: TABLET; ORAL
Strength: EQ 10MG BASE
Reference Listed Drug: No
Reference Standard: No
TE Code:
Application Number: A040207
Product Number: 002
Approval Date: May 1, 1997
Applicant Holder Full Name: DURAMED PHARMACEUTICALS INC SUB BARR LABORATORIES INC
Marketing Status:
Discontinued
Patent and Exclusivity Information
