Package 0904-5780-17

{"route": ["ORAL"], "spl_id": "2b99e188-08ce-4160-bf19-136bc4dd39be", "openfda": {"nui": ["N0000000151", "N0000175784"], "unii": ["5QZO15J2Z8"], "rxcui": ["310273"], "spl_set_id": ["ee0a263e-3f78-4534-9a30-803de636f92b"], "pharm_class_epc": ["Histamine-2 Receptor Antagonist [EPC]"], "pharm_class_moa": ["Histamine H2 Receptor Antagonists [MoA]"], "manufacturer_name": ["Major Pharmaceuticals"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "25 BLISTER PACK in 1 CARTON (0904-5780-17)  / 1 TABLET, FILM COATED in 1 BLISTER PACK", "package_ndc": "0904-5780-17", "marketing_start_date": "20061004"}, {"sample": false, "description": "1 BOTTLE in 1 CARTON (0904-5780-51)  / 50 TABLET, FILM COATED in 1 BOTTLE", "package_ndc": "0904-5780-51", "marketing_start_date": "20060929"}], "brand_name": "Major Heartburn Relief Maximum Strength", "product_id": "0904-5780_2b99e188-08ce-4160-bf19-136bc4dd39be", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Histamine H2 Receptor Antagonists [MoA]", "Histamine-2 Receptor Antagonist [EPC]"], "product_ndc": "0904-5780", "generic_name": "Famotidine", "labeler_name": "Major Pharmaceuticals", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Major Heartburn Relief", "brand_name_suffix": "Maximum Strength", "active_ingredients": [{"name": "FAMOTIDINE", "strength": "20 mg/1"}], "application_number": "ANDA077351", "marketing_category": "ANDA", "marketing_start_date": "20060929", "listing_expiration_date": "20261231"}