Package 11673-346-03

{"route": ["ORAL"], "spl_id": "dc644613-1131-499d-9c16-7ee241a10c26", "openfda": {"nui": ["N0000175525", "N0000000147", "N0000182140"], "unii": ["KG60484QX9"], "rxcui": ["402014"], "spl_set_id": ["7dc339da-e90b-452b-b25e-8d7f3aa8bc18"], "pharm_class_epc": ["Proton Pump Inhibitor [EPC]"], "pharm_class_moa": ["Proton Pump Inhibitors [MoA]", "Cytochrome P450 2C19 Inhibitors [MoA]"], "manufacturer_name": ["Target Corporation"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "3 BOTTLE in 1 CARTON (11673-346-03)  / 14 TABLET, DELAYED RELEASE in 1 BOTTLE", "package_ndc": "11673-346-03", "marketing_start_date": "20220203"}], "brand_name": "up and up omeprazole", "product_id": "11673-346_dc644613-1131-499d-9c16-7ee241a10c26", "dosage_form": "TABLET, DELAYED RELEASE", "pharm_class": ["Cytochrome P450 2C19 Inhibitors [MoA]", "Proton Pump Inhibitor [EPC]", "Proton Pump Inhibitors [MoA]"], "product_ndc": "11673-346", "generic_name": "omeprazole", "labeler_name": "Target Corporation", "product_type": "HUMAN OTC DRUG", "brand_name_base": "up and up omeprazole", "active_ingredients": [{"name": "OMEPRAZOLE", "strength": "20 mg/1"}], "application_number": "NDA022032", "marketing_category": "NDA", "marketing_start_date": "20220203", "listing_expiration_date": "20261231"}