Package 0904-6662-45

{"route": ["ORAL"], "spl_id": "a0df61ac-b037-40fc-a889-90de12c99010", "openfda": {"nui": ["N0000175525", "N0000000147", "N0000009724"], "unii": ["0K5C5T2QPG"], "rxcui": ["311277"], "spl_set_id": ["854e4235-4815-4461-9b9b-d3d783fb775d"], "pharm_class_pe": ["Inhibition Gastric Acid Secretion [PE]"], "pharm_class_epc": ["Proton Pump Inhibitor [EPC]"], "pharm_class_moa": ["Proton Pump Inhibitors [MoA]"], "manufacturer_name": ["Major Pharmaceuticals"]}, "finished": true, "packaging": [{"sample": false, "description": "80 BLISTER PACK in 1 CARTON (0904-6662-45)  / 1 CAPSULE, DELAYED RELEASE in 1 BLISTER PACK", "package_ndc": "0904-6662-45", "marketing_start_date": "20101015"}], "brand_name": "Lansoprazole", "product_id": "0904-6662_a0df61ac-b037-40fc-a889-90de12c99010", "dosage_form": "CAPSULE, DELAYED RELEASE", "pharm_class": ["Inhibition Gastric Acid Secretion [PE]", "Proton Pump Inhibitor [EPC]", "Proton Pump Inhibitors [MoA]"], "product_ndc": "0904-6662", "generic_name": "lansoprazole", "labeler_name": "Major Pharmaceuticals", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Lansoprazole", "active_ingredients": [{"name": "LANSOPRAZOLE", "strength": "30 mg/1"}], "application_number": "ANDA091269", "marketing_category": "ANDA", "marketing_start_date": "20101015", "listing_expiration_date": "20261231"}