Package 53746-735-90

{"route": ["ORAL"], "spl_id": "b9ac064d-eed2-4d3c-b984-c9ebcef68646", "openfda": {"nui": ["N0000175753", "N0000008486"], "unii": ["X72RBB02N8"], "rxcui": ["198358", "198359"], "spl_set_id": ["1aa40de5-c02d-49d6-8722-ed88c40c3ba6"], "pharm_class_pe": ["Decreased Central Nervous System Disorganized Electrical Activity [PE]"], "pharm_class_epc": ["Anti-epileptic Agent [EPC]"], "manufacturer_name": ["Amneal Pharmaceuticals of New York LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "180 TABLET in 1 BOTTLE (53746-735-18)", "package_ndc": "53746-735-18", "marketing_start_date": "20220810"}, {"sample": false, "description": "30 TABLET in 1 BOTTLE (53746-735-30)", "package_ndc": "53746-735-30", "marketing_start_date": "20220810"}, {"sample": false, "description": "90 TABLET in 1 BOTTLE (53746-735-90)", "package_ndc": "53746-735-90", "marketing_start_date": "20220810"}], "brand_name": "Felbamate", "product_id": "53746-735_b9ac064d-eed2-4d3c-b984-c9ebcef68646", "dosage_form": "TABLET", "pharm_class": ["Anti-epileptic Agent [EPC]", "Decreased Central Nervous System Disorganized Electrical Activity [PE]"], "product_ndc": "53746-735", "generic_name": "Felbamate", "labeler_name": "Amneal Pharmaceuticals of New York LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Felbamate", "active_ingredients": [{"name": "FELBAMATE", "strength": "600 mg/1"}], "application_number": "ANDA201680", "marketing_category": "ANDA", "marketing_start_date": "20220810", "listing_expiration_date": "20261231"}