Package 76420-859-75

{"route": ["ORAL"], "spl_id": "25322eee-f92a-5838-e063-6394a90aa376", "openfda": {"unii": ["Q42OMW3AT8", "804826J2HU"], "rxcui": ["617423", "617430"], "spl_set_id": ["fc5dc69a-3c23-49fc-b80f-1412aebc9b76"], "manufacturer_name": ["Asclemed USA, Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "100 mL in 1 BOTTLE (76420-859-01)", "package_ndc": "76420-859-01", "marketing_start_date": "20241024"}, {"sample": false, "description": "50 mL in 1 BOTTLE (76420-859-50)", "package_ndc": "76420-859-50", "marketing_start_date": "20241024"}, {"sample": false, "description": "75 mL in 1 BOTTLE (76420-859-75)", "package_ndc": "76420-859-75", "marketing_start_date": "20241024"}], "brand_name": "Amoxicillin and Clavulanate Potassium", "product_id": "76420-859_25322eee-f92a-5838-e063-6394a90aa376", "dosage_form": "POWDER, FOR SUSPENSION", "pharm_class": ["Penicillin-class Antibacterial [EPC]", "Penicillins [CS]", "beta Lactamase Inhibitor [EPC]", "beta Lactamase Inhibitors [MoA]"], "product_ndc": "76420-859", "generic_name": "Amoxicillin and Clavulanate Potassium", "labeler_name": "Asclemed USA, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Amoxicillin and Clavulanate Potassium", "active_ingredients": [{"name": "AMOXICILLIN", "strength": "200 mg/5mL"}, {"name": "CLAVULANATE POTASSIUM", "strength": "28.5 mg/5mL"}], "application_number": "ANDA201090", "marketing_category": "ANDA", "marketing_start_date": "20111220", "listing_expiration_date": "20261231"}