Package 68071-5065-3

{"route": ["ORAL"], "spl_id": "1b4353b9-db65-9ef4-e063-6394a90a4d30", "openfda": {"upc": ["0368071506532"], "unii": ["804826J2HU", "Q42OMW3AT8"], "rxcui": ["562508"], "spl_set_id": ["92ff1408-512c-d68d-e053-2a95a90adfbd"], "manufacturer_name": ["NuCare Pharmaceuticals,Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "3 TABLET, FILM COATED in 1 BOTTLE (68071-5065-3)", "package_ndc": "68071-5065-3", "marketing_start_date": "20190920"}, {"sample": false, "description": "4 TABLET, FILM COATED in 1 BOTTLE (68071-5065-4)", "package_ndc": "68071-5065-4", "marketing_start_date": "20190920"}], "brand_name": "Amoxicillin and Clavulanate Potassium", "product_id": "68071-5065_1b4353b9-db65-9ef4-e063-6394a90a4d30", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Penicillin-class Antibacterial [EPC]", "Penicillins [CS]", "beta Lactamase Inhibitor [EPC]", "beta Lactamase Inhibitors [MoA]"], "product_ndc": "68071-5065", "generic_name": "Amoxicillin and Clavulanate Potassium", "labeler_name": "NuCare Pharmaceuticals,Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Amoxicillin and Clavulanate Potassium", "active_ingredients": [{"name": "AMOXICILLIN", "strength": "875 mg/1"}, {"name": "CLAVULANATE POTASSIUM", "strength": "125 mg/1"}], "application_number": "ANDA091569", "marketing_category": "ANDA", "marketing_start_date": "20120120", "listing_expiration_date": "20261231"}