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Orange Book: Approved Drug Products with Therapeutic Equivalence Evaluations

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Product Details for ANDA 070801

HALOPERIDOL (HALOPERIDOL LACTATE)
EQ 5MG BASE/ML
Marketing Status: Discontinued
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: A070801
Product Number: 001
Approval Date: Dec 14, 1987
Applicant Holder Full Name: SOLOPAK LABORATORIES INC
Marketing Status:  Discontinued
Patent and Exclusivity Information
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