Package 80425-0174-1

{"route": ["ORAL"], "spl_id": "2a99b1dd-bed3-79f9-e063-6394a90a35f3", "openfda": {"nui": ["N0000175525", "N0000000147", "N0000009724"], "unii": ["0K5C5T2QPG"], "rxcui": ["311277"], "spl_set_id": ["ce1a4f32-da65-29d3-e053-2995a90a42ee"], "pharm_class_pe": ["Inhibition Gastric Acid Secretion [PE]"], "pharm_class_epc": ["Proton Pump Inhibitor [EPC]"], "pharm_class_moa": ["Proton Pump Inhibitors [MoA]"], "manufacturer_name": ["Advanced Rx Pharmacy of Tennessee, LLC"]}, "finished": true, "packaging": [{"sample": false, "description": "30 CAPSULE, DELAYED RELEASE in 1 BOTTLE (80425-0174-1)", "package_ndc": "80425-0174-1", "marketing_start_date": "20180604"}], "brand_name": "Lansoprazole DR", "product_id": "80425-0174_2a99b1dd-bed3-79f9-e063-6394a90a35f3", "dosage_form": "CAPSULE, DELAYED RELEASE", "pharm_class": ["Inhibition Gastric Acid Secretion [PE]", "Proton Pump Inhibitor [EPC]", "Proton Pump Inhibitors [MoA]"], "product_ndc": "80425-0174", "generic_name": "Lansoprazole", "labeler_name": "Advanced Rx Pharmacy of Tennessee, LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Lansoprazole", "brand_name_suffix": "DR", "active_ingredients": [{"name": "LANSOPRAZOLE", "strength": "30 mg/1"}], "application_number": "ANDA205868", "marketing_category": "ANDA", "marketing_start_date": "20180604", "listing_expiration_date": "20261231"}