Package 81964-203-51

{"route": ["ORAL"], "spl_id": "3a120204-39ce-43cd-e063-6394a90a9f19", "openfda": {"upc": ["0381964203691", "0381964203547"], "unii": ["804826J2HU", "Q42OMW3AT8"], "rxcui": ["617993"], "spl_set_id": ["7d4dfd6f-bd1a-4acc-8506-07fca08f8a38"], "manufacturer_name": ["USAntibiotics, LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "75 mL in 1 BOTTLE (81964-203-51)", "package_ndc": "81964-203-51", "marketing_start_date": "20220919"}, {"sample": false, "description": "200 mL in 1 BOTTLE (81964-203-54)", "package_ndc": "81964-203-54", "marketing_start_date": "20220919"}, {"sample": false, "description": "125 mL in 1 BOTTLE (81964-203-69)", "package_ndc": "81964-203-69", "marketing_start_date": "20220919"}], "brand_name": "AMOXICILLIN AND CLAVULANATE POTASSIUM", "product_id": "81964-203_3a120204-39ce-43cd-e063-6394a90a9f19", "dosage_form": "FOR SUSPENSION", "pharm_class": ["Penicillin-class Antibacterial [EPC]", "Penicillins [CS]", "beta Lactamase Inhibitor [EPC]", "beta Lactamase Inhibitors [MoA]"], "product_ndc": "81964-203", "generic_name": "amoxicillin and clavulanate potassium", "labeler_name": "USAntibiotics, LLC", "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": "NDA050755", "marketing_category": "NDA AUTHORIZED GENERIC", "marketing_start_date": "20220919", "listing_expiration_date": "20261231"}