Active Ingredient: HALOPERIDOL LACTATE
Proprietary Name: HALDOL
Dosage Form; Route of Administration: CONCENTRATE; ORAL
Strength: EQ 2MG BASE/ML **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Reference Listed Drug: Yes
Reference Standard: No
TE Code:
Application Number: N015922
Product Number: 001
Approval Date: Approved Prior to Jan 1, 1982
Applicant Holder Full Name: ORTHO MCNEIL PHARMACEUTICAL
Marketing Status:
Discontinued
Patent and Exclusivity Information