Package 73043-010-02

{"route": ["ORAL"], "spl_id": "e5eda5f6-317c-43ac-b1d7-c6ce635593da", "openfda": {"unii": ["804826J2HU", "Q42OMW3AT8"], "rxcui": ["617322"], "spl_set_id": ["b0b2e164-e70d-471f-92ce-abdac6cb405f"], "manufacturer_name": ["Devatis, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "75 mL in 1 BOTTLE (73043-010-01)", "package_ndc": "73043-010-01", "marketing_start_date": "20240815"}, {"sample": false, "description": "100 mL in 1 BOTTLE (73043-010-02)", "package_ndc": "73043-010-02", "marketing_start_date": "20240901"}, {"sample": false, "description": "150 mL in 1 BOTTLE (73043-010-03)", "package_ndc": "73043-010-03", "marketing_start_date": "20240705"}], "brand_name": "amoxicillin and clavulanate potassium", "product_id": "73043-010_e5eda5f6-317c-43ac-b1d7-c6ce635593da", "dosage_form": "POWDER, FOR SUSPENSION", "pharm_class": ["Penicillin-class Antibacterial [EPC]", "Penicillins [CS]", "beta Lactamase Inhibitor [EPC]", "beta Lactamase Inhibitors [MoA]"], "product_ndc": "73043-010", "generic_name": "amoxicillin and clavulanate potassium", "labeler_name": "Devatis, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "amoxicillin and clavulanate potassium", "active_ingredients": [{"name": "AMOXICILLIN", "strength": "250 mg/5mL"}, {"name": "CLAVULANATE POTASSIUM", "strength": "62.5 mg/5mL"}], "application_number": "ANDA210374", "marketing_category": "ANDA", "marketing_start_date": "20240705", "listing_expiration_date": "20261231"}