Package 63304-644-69

{"route": ["ORAL"], "spl_id": "8c155c45-e5c8-4358-90da-8f6d193ad88b", "openfda": {"nui": ["N0000175430"], "upc": ["0363304949308"], "unii": ["L6UH7ZF8HC"], "rxcui": ["401953", "401954", "403825", "616698", "616705"], "spl_set_id": ["f91f551e-926f-440d-83d2-357e9d7484fe"], "pharm_class_epc": ["Atypical Antipsychotic [EPC]"], "manufacturer_name": ["Sun Pharmaceutical Industries, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "500 TABLET, ORALLY DISINTEGRATING in 1 BOTTLE (63304-644-05)", "package_ndc": "63304-644-05", "marketing_start_date": "20100806"}, {"sample": false, "description": "1 POUCH in 1 BOX, UNIT-DOSE (63304-644-17)  / 1 TABLET, ORALLY DISINTEGRATING in 1 POUCH (63304-644-11)", "package_ndc": "63304-644-17", "marketing_start_date": "20100806"}, {"sample": false, "description": "30 TABLET, ORALLY DISINTEGRATING in 1 BOTTLE (63304-644-30)", "package_ndc": "63304-644-30", "marketing_start_date": "20100806"}, {"sample": false, "description": "1 BLISTER PACK in 1 CARTON (63304-644-69)  / 10 TABLET, ORALLY DISINTEGRATING in 1 BLISTER PACK", "package_ndc": "63304-644-69", "marketing_start_date": "20100806"}], "brand_name": "Risperidone", "product_id": "63304-644_8c155c45-e5c8-4358-90da-8f6d193ad88b", "dosage_form": "TABLET, ORALLY DISINTEGRATING", "pharm_class": ["Atypical Antipsychotic [EPC]"], "product_ndc": "63304-644", "generic_name": "Risperidone", "labeler_name": "Sun Pharmaceutical Industries, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Risperidone", "active_ingredients": [{"name": "RISPERIDONE", "strength": "4 mg/1"}], "application_number": "ANDA078474", "marketing_category": "ANDA", "marketing_start_date": "20100806", "listing_expiration_date": "20261231"}