FDA Drug Application (075523) for NALOXONE HYDROCHLORIDE AND PENTAZOCINE HYDROCHLORIDE by SUN PHARM INDS LTD

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Application Number075523
Product Number001
FormTABLET;ORAL
DosageEQ 0.5MG BASE;EQ 50MG BASE
Product Market Status Prescription
Therapeutic Equivalence Evaluation Code AB Products meeting necessary bioequivalence requirements
Reference Drug
Drug NameNALOXONE HYDROCHLORIDE AND PENTAZOCINE HYDROCHLORIDE
Active IngredientNALOXONE HYDROCHLORIDE; PENTAZOCINE HYDROCHLORIDE



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