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: A089485
Product Number: 001
Approval Date: Jan 20, 1987
Applicant Holder Full Name: DURAMED PHARMACEUTICALS INC SUB BARR LABORATORIES INC
Marketing Status:
Discontinued
Patent and Exclusivity Information
