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: AB
Application Number: A216495
Product Number: 002
Approval Date: Aug 8, 2022
Applicant Holder Full Name: ZYDUS LIFESCIENCES GLOBAL FZE
Marketing Status:
Prescription
Patent and Exclusivity Information