Package 70518-4034-0

{"route": ["ORAL"], "spl_id": "45c15571-71e0-c60a-e063-6294a90a5eef", "openfda": {"nui": ["N0000175495", "M0361132"], "unii": ["ISQ9I6J12J"], "rxcui": ["311347"], "spl_set_id": ["3e0d868d-f419-47e8-a3bc-41ececac468b"], "pharm_class_cs": ["Oxazolidinones [CS]"], "pharm_class_epc": ["Oxazolidinone Antibacterial [EPC]"], "manufacturer_name": ["REMEDYREPACK INC."]}, "finished": true, "packaging": [{"sample": false, "description": "20 TABLET, FILM COATED in 1 BOTTLE (70518-4034-0)", "package_ndc": "70518-4034-0", "marketing_start_date": "20240508"}, {"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70518-4034-1)", "package_ndc": "70518-4034-1", "marketing_start_date": "20251212"}], "brand_name": "Linezolid", "product_id": "70518-4034_45c15571-71e0-c60a-e063-6294a90a5eef", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Oxazolidinone Antibacterial [EPC]", "Oxazolidinones [CS]"], "product_ndc": "70518-4034", "generic_name": "Linezolid", "labeler_name": "REMEDYREPACK INC.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Linezolid", "active_ingredients": [{"name": "LINEZOLID", "strength": "600 mg/1"}], "application_number": "ANDA205517", "marketing_category": "ANDA", "marketing_start_date": "20240508", "listing_expiration_date": "20261231"}