Package 65841-731-16

{"route": ["ORAL"], "spl_id": "36fa833c-716f-4b69-9326-3c54753240dc", "openfda": {"unii": ["3ST302B24A"], "rxcui": ["979480", "979485", "979492"], "spl_set_id": ["9ccd6823-e813-472c-99cd-c6ef25e74bed"], "manufacturer_name": ["Zydus Lifesciences Limited"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET, FILM COATED in 1 BOTTLE (65841-731-01)", "package_ndc": "65841-731-01", "marketing_start_date": "20101004"}, {"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE (65841-731-06)", "package_ndc": "65841-731-06", "marketing_start_date": "20101004"}, {"sample": false, "description": "1000 TABLET, FILM COATED in 1 BOTTLE (65841-731-10)", "package_ndc": "65841-731-10", "marketing_start_date": "20101004"}, {"sample": false, "description": "90 TABLET, FILM COATED in 1 BOTTLE (65841-731-16)", "package_ndc": "65841-731-16", "marketing_start_date": "20101004"}, {"sample": false, "description": "10 BLISTER PACK in 1 CARTON (65841-731-77)  / 10 TABLET, FILM COATED in 1 BLISTER PACK (65841-731-30)", "package_ndc": "65841-731-77", "marketing_start_date": "20101004"}], "brand_name": "Losartan Potassium", "product_id": "65841-731_36fa833c-716f-4b69-9326-3c54753240dc", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Angiotensin 2 Receptor Antagonists [MoA]", "Angiotensin 2 Receptor Blocker [EPC]"], "product_ndc": "65841-731", "generic_name": "Losartan Potassium", "labeler_name": "Zydus Lifesciences Limited", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Losartan Potassium", "active_ingredients": [{"name": "LOSARTAN POTASSIUM", "strength": "100 mg/1"}], "application_number": "ANDA078243", "marketing_category": "ANDA", "marketing_start_date": "20101004", "listing_expiration_date": "20271231"}