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: A216595
Product Number: 002
Approval Date: Mar 17, 2023
Applicant Holder Full Name: GLENMARK PHARMACEUTICALS LTD
Marketing Status:
Prescription
Patent and Exclusivity Information