Active Ingredient: HALOPERIDOL LACTATE
Proprietary Name: HALOPERIDOL
Dosage Form; Route of Administration: INJECTABLE; INJECTION
Strength: EQ 5MG BASE/ML
Reference Listed Drug: No
Reference Standard: No
TE Code:
Application Number: A070802
Product Number: 001
Approval Date: Dec 14, 1987
Applicant Holder Full Name: SMITH AND NEPHEW SOLOPAK DIV SMITH AND NEPHEW
Marketing Status:
Discontinued
Patent and Exclusivity Information