Active Ingredient: HALOPERIDOL
Proprietary Name: HALOPERIDOL
Dosage Form; Route of Administration: TABLET; ORAL
Strength: 2MG
Reference Listed Drug: No
Reference Standard: No
TE Code: AB
Application Number: A071130
Product Number: 001
Approval Date: Feb 17, 1987
Applicant Holder Full Name: SCIEGEN PHARMACEUTICALS INC
Marketing Status:
Prescription
Patent and Exclusivity Information