Active Ingredient: PROCHLORPERAZINE
Proprietary Name: PROCHLORPERAZINE
Dosage Form; Route of Administration: SUPPOSITORY; RECTAL
Strength: 25MG
Reference Listed Drug: No
Reference Standard: Yes
TE Code: AB
Application Number: A040058
Product Number: 001
Approval Date: Nov 24, 1993
Applicant Holder Full Name: COSETTE PHARMACEUTICALS INC
Marketing Status:
Prescription
Patent and Exclusivity Information