FDA Drug Application (077101) for QUASENSE by WATSON LABS

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Application Number077101
Product Number001
FormTABLET;ORAL
Dosage0.03MG;0.15MG
Product Market Status Prescription
Therapeutic Equivalence Evaluation Code AB Products meeting necessary bioequivalence requirements
Reference Drug
Drug NameQUASENSE
Active IngredientETHINYL ESTRADIOL; LEVONORGESTREL



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