Package 71297-240-35

{"route": ["ORAL"], "spl_id": "18975386-c292-a0cb-e063-6294a90aed18", "openfda": {"upc": ["0371297240364", "0371297240340"], "unii": ["804826J2HU", "Q42OMW3AT8"], "rxcui": ["617302", "617333"], "spl_set_id": ["04a31a42-d79e-bbb4-e063-6394a90a63ee"], "manufacturer_name": ["Allegis Holdings, LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "75 mL in 1 BOTTLE (71297-240-34)", "package_ndc": "71297-240-34", "marketing_start_date": "20240220"}, {"sample": false, "description": "100 mL in 1 BOTTLE (71297-240-35)", "package_ndc": "71297-240-35", "marketing_start_date": "20230901"}, {"sample": false, "description": "150 mL in 1 BOTTLE (71297-240-36)", "package_ndc": "71297-240-36", "marketing_start_date": "20230901"}], "brand_name": "Augmentin", "product_id": "71297-240_18975386-c292-a0cb-e063-6294a90aed18", "dosage_form": "FOR SUSPENSION", "pharm_class": ["Penicillin-class Antibacterial [EPC]", "Penicillins [CS]", "beta Lactamase Inhibitor [EPC]", "beta Lactamase Inhibitors [MoA]"], "product_ndc": "71297-240", "generic_name": "Amoxicillin and Clavulanate Potassium", "labeler_name": "Allegis Holdings, LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Augmentin", "active_ingredients": [{"name": "AMOXICILLIN", "strength": "125 mg/5mL"}, {"name": "CLAVULANATE POTASSIUM", "strength": "31.25 mg/5mL"}], "application_number": "NDA050575", "marketing_category": "NDA", "marketing_start_date": "20230901", "listing_expiration_date": "20261231"}