Package 72189-281-20

{"route": ["ORAL"], "spl_id": "2c2908f5-e111-e912-e063-6294a90a01c9", "openfda": {"unii": ["804826J2HU", "Q42OMW3AT8"], "rxcui": ["617296"], "spl_set_id": ["cdc6d30a-754e-6672-e053-2a95a90afa7f"], "manufacturer_name": ["DirectRx"]}, "finished": true, "packaging": [{"sample": false, "description": "14 TABLET, FILM COATED in 1 BOTTLE (72189-281-14)", "package_ndc": "72189-281-14", "marketing_start_date": "20211007"}, {"sample": false, "description": "20 TABLET, FILM COATED in 1 BOTTLE (72189-281-20)", "package_ndc": "72189-281-20", "marketing_start_date": "20211007"}], "brand_name": "AMOXICILLIN AND CLAVULANATE POTASSIUM", "product_id": "72189-281_2c2908f5-e111-e912-e063-6294a90a01c9", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Penicillin-class Antibacterial [EPC]", "Penicillins [CS]", "beta Lactamase Inhibitor [EPC]", "beta Lactamase Inhibitors [MoA]"], "product_ndc": "72189-281", "generic_name": "AMOXICILLIN AND CLAVULANATE POTASSIUM", "labeler_name": "DirectRx", "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": "20211007", "listing_expiration_date": "20261231"}