Package 72189-543-20

{"route": ["ORAL"], "spl_id": "138d9ed1-2f90-d19d-e063-6394a90a695d", "openfda": {"nui": ["N0000000151", "N0000175784"], "unii": ["5QZO15J2Z8"], "rxcui": ["310273"], "spl_set_id": ["138d9ed1-2f8f-d19d-e063-6394a90a695d"], "pharm_class_epc": ["Histamine-2 Receptor Antagonist [EPC]"], "pharm_class_moa": ["Histamine H2 Receptor Antagonists [MoA]"], "manufacturer_name": ["Direct_Rx"]}, "finished": true, "packaging": [{"sample": false, "description": "20 TABLET, FILM COATED in 1 BOTTLE (72189-543-20)", "package_ndc": "72189-543-20", "marketing_start_date": "20240313"}, {"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE (72189-543-30)", "package_ndc": "72189-543-30", "marketing_start_date": "20240313"}], "brand_name": "Famotidine", "product_id": "72189-543_138d9ed1-2f90-d19d-e063-6394a90a695d", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Histamine H2 Receptor Antagonists [MoA]", "Histamine-2 Receptor Antagonist [EPC]"], "product_ndc": "72189-543", "generic_name": "Famotidine", "labeler_name": "Direct_Rx", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Famotidine", "active_ingredients": [{"name": "FAMOTIDINE", "strength": "20 mg/1"}], "application_number": "ANDA075718", "marketing_category": "ANDA", "marketing_start_date": "20240313", "listing_expiration_date": "20261231"}