Package 71610-207-30

{"route": ["ORAL"], "spl_id": "efa818c7-3f30-4f41-9071-71e298ae171d", "openfda": {"unii": ["3ST302B24A"], "rxcui": ["979492"], "spl_set_id": ["1f55aaa2-5848-47e0-bba0-6a70b2fa05dd"], "manufacturer_name": ["Aphena Pharma Solutions - Tennessee, LLC"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE (71610-207-30)", "package_ndc": "71610-207-30", "marketing_start_date": "20181214"}, {"sample": false, "description": "45 TABLET, FILM COATED in 1 BOTTLE (71610-207-45)", "package_ndc": "71610-207-45", "marketing_start_date": "20181214"}, {"sample": false, "description": "90 TABLET, FILM COATED in 1 BOTTLE (71610-207-60)", "package_ndc": "71610-207-60", "marketing_start_date": "20181214"}], "brand_name": "Losartan Potassium", "product_id": "71610-207_efa818c7-3f30-4f41-9071-71e298ae171d", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Angiotensin 2 Receptor Antagonists [MoA]", "Angiotensin 2 Receptor Blocker [EPC]"], "product_ndc": "71610-207", "generic_name": "Losartan potassium", "labeler_name": "Aphena Pharma Solutions - Tennessee, LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Losartan Potassium", "active_ingredients": [{"name": "LOSARTAN POTASSIUM", "strength": "50 mg/1"}], "application_number": "ANDA091497", "marketing_category": "ANDA", "marketing_start_date": "20140730", "listing_expiration_date": "20261231"}