FDA Drug Approval, A203594, DROSPIRENONE, ETHINYL ESTRADIOL AND LEVOMEFOLATE CALCIUM

FDA Drug Approval, A203594, DROSPIRENONE, ETHINYL ESTRADIOL AND LEVOMEFOLATE CALCIUM

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ANDA: 203594
Company: WATSON LABS INC
Drug Name: DROSPIRENONE, ETHINYL ESTRADIOL AND LEVOMEFOLATE CALCIUM
Active Ingredients: DROSPIRENONE; ETHINYL ESTRADIOL; LEVOMEFOLATE CALCIUM
Strength: 3MG,N/A;0.03MG,N/A;0.451MG,0.451MG
Dosage Form/Route: TABLET;ORAL
Action Date: 10/11/2016
Marketing Status: Prescription
Submission Classification: ORIG-1 TE Code: AB
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