FDA Drug Application (009388) for DIAMOX by TEVA WOMENS

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Application Number009388
Product Number001
FormINJECTABLE;INJECTION
DosageEQ 500MG BASE/VIAL **Federal Register determination that product was not discontinued or withdrawn for safety or efficacy reasons**
Product Market Status Discontinued
Therapeutic Equivalence Evaluation Code
Reference Drug
Drug NameDIAMOX
Active IngredientACETAZOLAMIDE SODIUM



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