Package 68071-2355-5

{"route": ["ORAL"], "spl_id": "4b34eb00-41fb-6778-e063-6394a90a832a", "openfda": {"upc": ["0368071235555"], "unii": ["804826J2HU", "Q42OMW3AT8"], "rxcui": ["617993"], "spl_set_id": ["bcd19a89-e9dc-b85f-e053-2a95a90a6f3e"], "manufacturer_name": ["NuCare Pharmaceuticals,Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "75 mL in 1 BOTTLE (68071-2355-5)", "package_ndc": "68071-2355-5", "marketing_start_date": "20210305"}], "brand_name": "Amoxicillin and Clavulanate Potassium", "product_id": "68071-2355_4b34eb00-41fb-6778-e063-6394a90a832a", "dosage_form": "POWDER, FOR SUSPENSION", "pharm_class": ["Penicillin-class Antibacterial [EPC]", "Penicillins [CS]", "beta Lactamase Inhibitor [EPC]", "beta Lactamase Inhibitors [MoA]"], "product_ndc": "68071-2355", "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": "600 mg/5mL"}, {"name": "CLAVULANATE POTASSIUM", "strength": "42.9 mg/5mL"}], "application_number": "ANDA201091", "marketing_category": "ANDA", "marketing_start_date": "20111220", "listing_expiration_date": "20271231"}