Package 0173-0778-00

{"spl_id": "4492fd3c-e068-4599-8a10-0b26ea2a4f91", "openfda": {"nui": ["N0000175753", "N0000008486", "N0000175751", "N0000187061", "N0000000191"], "upc": ["0301730526007", "0301730644602", "0301730699008", "0301730642554", "0301730643605", "0301730527004"], "unii": ["U3H27498KS"], "rxcui": ["103968", "105018", "105019", "108782", "198427", "198428", "198429", "198430", "201239", "201240", "206201", "252478", "252479", "282401", "311264", "311265", "349010", "542426", "751139", "751563", "753451", "795772", "795774", "795778", "849049", "849050", "849051", "849052", "851748", "851749", "851750", "851751", "851752", "851753"], "spl_set_id": ["d7e3572d-56fe-4727-2bb4-013ccca22678"], "pharm_class_pe": ["Decreased Central Nervous System Disorganized Electrical Activity [PE]"], "pharm_class_epc": ["Anti-epileptic Agent [EPC]", "Mood Stabilizer [EPC]"], "pharm_class_moa": ["Organic Cation Transporter 2 Inhibitors [MoA]", "Dihydrofolate Reductase Inhibitors [MoA]"], "manufacturer_name": ["GlaxoSmithKline LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 BLISTER PACK in 1 PACKAGE, COMBINATION (0173-0778-00)  / 1 KIT in 1 BLISTER PACK", "package_ndc": "0173-0778-00", "marketing_start_date": "20090605"}], "brand_name": "LAMICTAL ODT", "product_id": "0173-0778_4492fd3c-e068-4599-8a10-0b26ea2a4f91", "dosage_form": "KIT", "product_ndc": "0173-0778", "generic_name": "lamotrigine", "labeler_name": "GlaxoSmithKline LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "LAMICTAL", "brand_name_suffix": "ODT", "application_number": "NDA022251", "marketing_category": "NDA", "marketing_start_date": "20090605", "listing_expiration_date": "20261231"}