Package 51672-4131-6

{"route": ["ORAL"], "spl_id": "44812d3c-0fc0-67dd-e063-6394a90a9d70", "openfda": {"nui": ["N0000175753", "N0000008486", "N0000175751", "N0000187061", "N0000000191"], "upc": ["0351672413019", "0351672413347", "0351672413248", "0351672413118"], "unii": ["U3H27498KS"], "rxcui": ["198427", "198428", "198429", "282401"], "spl_set_id": ["b829f9b2-f0ac-408a-a6f4-18b72150227d"], "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": ["Sun Pharmaceutical Industries, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "10 BLISTER PACK in 1 CARTON (51672-4131-0)  / 10 TABLET in 1 BLISTER PACK", "package_ndc": "51672-4131-0", "marketing_start_date": "20090127"}, {"sample": false, "description": "100 TABLET in 1 BOTTLE (51672-4131-1)", "package_ndc": "51672-4131-1", "marketing_start_date": "20090127"}, {"sample": false, "description": "1000 TABLET in 1 BOTTLE (51672-4131-3)", "package_ndc": "51672-4131-3", "marketing_start_date": "20090127"}, {"sample": false, "description": "60 TABLET in 1 BOTTLE (51672-4131-4)", "package_ndc": "51672-4131-4", "marketing_start_date": "20090127"}, {"sample": false, "description": "30 TABLET in 1 BOTTLE (51672-4131-6)", "package_ndc": "51672-4131-6", "marketing_start_date": "20090127"}], "brand_name": "Lamotrigine", "product_id": "51672-4131_44812d3c-0fc0-67dd-e063-6394a90a9d70", "dosage_form": "TABLET", "pharm_class": ["Anti-epileptic Agent [EPC]", "Decreased Central Nervous System Disorganized Electrical Activity [PE]", "Dihydrofolate Reductase Inhibitors [MoA]", "Mood Stabilizer [EPC]", "Organic Cation Transporter 2 Inhibitors [MoA]"], "product_ndc": "51672-4131", "generic_name": "Lamotrigine", "labeler_name": "Sun Pharmaceutical Industries, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Lamotrigine", "active_ingredients": [{"name": "LAMOTRIGINE", "strength": "100 mg/1"}], "application_number": "ANDA078525", "marketing_category": "ANDA", "marketing_start_date": "20090127", "listing_expiration_date": "20261231"}