Package 59651-025-01

{"route": ["ORAL"], "spl_id": "8c4f5611-f65b-42c2-8412-e616f149ee90", "openfda": {"unii": ["Q42OMW3AT8", "804826J2HU"], "rxcui": ["617302", "617322"], "spl_set_id": ["3ae0c95f-7ffa-4317-9fea-4d07b86bee72"], "manufacturer_name": ["Aurobindo Pharma Limited"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 mL in 1 BOTTLE (59651-025-01)", "package_ndc": "59651-025-01", "marketing_start_date": "20190419"}, {"sample": false, "description": "150 mL in 1 BOTTLE (59651-025-55)", "package_ndc": "59651-025-55", "marketing_start_date": "20190419"}, {"sample": false, "description": "75 mL in 1 BOTTLE (59651-025-75)", "package_ndc": "59651-025-75", "marketing_start_date": "20190419"}], "brand_name": "Amoxicillin and Clavulanate Potassium", "product_id": "59651-025_8c4f5611-f65b-42c2-8412-e616f149ee90", "dosage_form": "POWDER, FOR SUSPENSION", "pharm_class": ["Penicillin-class Antibacterial [EPC]", "Penicillins [CS]", "beta Lactamase Inhibitor [EPC]", "beta Lactamase Inhibitors [MoA]"], "product_ndc": "59651-025", "generic_name": "Amoxicillin and Clavulanate Potassium", "labeler_name": "Aurobindo Pharma Limited", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Amoxicillin and Clavulanate Potassium", "active_ingredients": [{"name": "AMOXICILLIN", "strength": "125 mg/5mL"}, {"name": "CLAVULANATE POTASSIUM", "strength": "31.25 mg/5mL"}], "application_number": "ANDA209371", "marketing_category": "ANDA", "marketing_start_date": "20190419", "listing_expiration_date": "20261231"}