FDA Drug Application (015922) for HALDOL by ORTHO MCNEIL

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Application Number015922
Product Number001
FormCONCENTRATE;ORAL
DosageEQ 2MG BASE/ML
Product Market Status Discontinued
Therapeutic Equivalence Evaluation Code
Reference Drug
Drug NameHALDOL
Active IngredientHALOPERIDOL LACTATE



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