Package 0781-1831-20

{"route": ["ORAL"], "spl_id": "6a6233c9-2bba-4d8c-9bfa-e5c5055cf91f", "openfda": {"upc": ["0307816102462", "0307811831206", "0307811874319", "0307811852201"], "unii": ["Q42OMW3AT8", "804826J2HU"], "rxcui": ["562251", "562508", "617296", "617423", "617430"], "spl_set_id": ["7cba82f0-9886-46e9-8dbd-43a448aade29"], "manufacturer_name": ["Sandoz Inc"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET, FILM COATED in 1 BOTTLE (0781-1831-01)", "package_ndc": "0781-1831-01", "marketing_start_date": "20220920"}, {"sample": false, "description": "100 TABLET, FILM COATED in 1 BOX, UNIT-DOSE (0781-1831-13)", "package_ndc": "0781-1831-13", "marketing_start_date": "20020315"}, {"sample": false, "description": "20 TABLET, FILM COATED in 1 BOTTLE (0781-1831-20)", "package_ndc": "0781-1831-20", "marketing_start_date": "20020315"}], "brand_name": "Amoxicillin and Clavulanate Potassium", "product_id": "0781-1831_6a6233c9-2bba-4d8c-9bfa-e5c5055cf91f", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Penicillin-class Antibacterial [EPC]", "Penicillins [CS]", "beta Lactamase Inhibitor [EPC]", "beta Lactamase Inhibitors [MoA]"], "product_ndc": "0781-1831", "generic_name": "Amoxicillin and Clavulanate Potassium", "labeler_name": "Sandoz Inc", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Amoxicillin and Clavulanate Potassium", "active_ingredients": [{"name": "AMOXICILLIN", "strength": "500 mg/1"}, {"name": "CLAVULANATE POTASSIUM", "strength": "125 mg/1"}], "application_number": "ANDA065064", "marketing_category": "ANDA", "marketing_start_date": "20020315", "listing_expiration_date": "20261231"}