Package 68788-8307-2

{"route": ["ORAL"], "spl_id": "23c2896b-d08f-4948-ac77-e15df706eeac", "openfda": {"unii": ["804826J2HU", "Q42OMW3AT8"], "rxcui": ["562508"], "spl_set_id": ["1b8a6312-ae47-45fb-ba5e-eedbc176afa0"], "manufacturer_name": ["Preferred Pharmaceuticals Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "20 TABLET, COATED in 1 BOTTLE (68788-8307-2)", "package_ndc": "68788-8307-2", "marketing_start_date": "20221220"}], "brand_name": "AMOXICILLIN AND CLAVULANATE POTASSIUM", "product_id": "68788-8307_23c2896b-d08f-4948-ac77-e15df706eeac", "dosage_form": "TABLET, COATED", "pharm_class": ["Penicillin-class Antibacterial [EPC]", "Penicillins [CS]", "beta Lactamase Inhibitor [EPC]", "beta Lactamase Inhibitors [MoA]"], "product_ndc": "68788-8307", "generic_name": "amoxicillin and clavulanate potassium", "labeler_name": "Preferred 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": "NDA050720", "marketing_category": "NDA AUTHORIZED GENERIC", "marketing_start_date": "20221220", "listing_expiration_date": "20271231"}