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DosageEQ 500MG BASE/VIAL **Federal Register determination that product was not discontinued or withdrawn for safety or efficacy reasons**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

Active IngredientCount
List of drugs with Active Ingredient ACETAZOLAMIDE2
List of drugs with Active Ingredient ACETAZOLAMIDE SODIUM2


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