Package 50090-0713-0

{"route": ["ORAL"], "spl_id": "ad315af7-46fa-4b63-a48c-351e3f0c3b18", "openfda": {"unii": ["804826J2HU"], "rxcui": ["308192", "308194"], "spl_set_id": ["c3d3f94f-e976-4625-9667-3d716932f2fa"], "manufacturer_name": ["A-S Medication Solutions"]}, "finished": true, "packaging": [{"sample": false, "description": "20 TABLET, FILM COATED in 1 BOTTLE (50090-0713-0)", "package_ndc": "50090-0713-0", "marketing_start_date": "20141128"}, {"sample": false, "description": "14 TABLET, FILM COATED in 1 BOTTLE (50090-0713-1)", "package_ndc": "50090-0713-1", "marketing_start_date": "20180606"}, {"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE (50090-0713-2)", "package_ndc": "50090-0713-2", "marketing_start_date": "20141128"}], "brand_name": "Amoxicillin", "product_id": "50090-0713_ad315af7-46fa-4b63-a48c-351e3f0c3b18", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Penicillin-class Antibacterial [EPC]", "Penicillins [CS]"], "product_ndc": "50090-0713", "generic_name": "Amoxicillin", "labeler_name": "A-S Medication Solutions", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Amoxicillin", "active_ingredients": [{"name": "AMOXICILLIN", "strength": "875 mg/1"}], "application_number": "ANDA065256", "marketing_category": "ANDA", "marketing_start_date": "20051109", "listing_expiration_date": "20261231"}