Active Ingredient: HALOPERIDOL
Proprietary Name: HALOPERIDOL
Dosage Form; Route of Administration: TABLET; ORAL
Strength: 20MG
Reference Listed Drug: No
Reference Standard: No
TE Code: AB
Application Number: A071211
Product Number: 001
Approval Date: Mar 11, 1988
Applicant Holder Full Name: CHARTWELL RX SCIENCES LLC
Marketing Status:
Prescription
Patent and Exclusivity Information