Package 68788-0483-7

{"route": ["ORAL"], "spl_id": "e51cf486-cd20-464d-a9e5-917ee699ad43", "openfda": {"unii": ["804826J2HU", "Q42OMW3AT8"], "rxcui": ["617993"], "spl_set_id": ["22a387bd-92ce-4ebc-b475-20d7750a2507"], "manufacturer_name": ["Preferred Pharmaceuticals, Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "125 mL in 1 BOTTLE (68788-0483-1)", "package_ndc": "68788-0483-1", "marketing_start_date": "20111107"}, {"sample": false, "description": "75 mL in 1 BOTTLE (68788-0483-7)", "package_ndc": "68788-0483-7", "marketing_start_date": "20111107"}], "brand_name": "Amoxicillin and Clavulanate Potassium", "product_id": "68788-0483_e51cf486-cd20-464d-a9e5-917ee699ad43", "dosage_form": "POWDER, FOR SUSPENSION", "pharm_class": ["Penicillin-class Antibacterial [EPC]", "Penicillins [CS]", "beta Lactamase Inhibitor [EPC]", "beta Lactamase Inhibitors [MoA]"], "product_ndc": "68788-0483", "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": "600 mg/5mL"}, {"name": "CLAVULANATE POTASSIUM", "strength": "42.9 mg/5mL"}], "application_number": "ANDA201091", "marketing_category": "ANDA", "marketing_start_date": "20111107", "listing_expiration_date": "20271231"}