Package 43598-550-30

{"route": ["ORAL"], "spl_id": "4007a0a9-7228-1cd4-e063-6394a90a85bf", "openfda": {"nui": ["N0000175753", "N0000008486", "N0000175751", "N0000187061", "N0000000191"], "upc": ["0343598551302", "0343598550015", "0343598553306", "0343598550305", "0343598552309"], "unii": ["U3H27498KS"], "rxcui": ["103968", "198430", "252478", "252479"], "spl_set_id": ["54ea1ec3-876b-4d3a-a92b-1a6d70951de0"], "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": ["Dr. Reddys Laboratories Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET, ORALLY DISINTEGRATING in 1 BOTTLE (43598-550-01)", "package_ndc": "43598-550-01", "marketing_start_date": "20160617"}, {"sample": false, "description": "30 TABLET, ORALLY DISINTEGRATING in 1 BOTTLE (43598-550-30)", "package_ndc": "43598-550-30", "marketing_start_date": "20160617"}], "brand_name": "Lamotrigine", "product_id": "43598-550_4007a0a9-7228-1cd4-e063-6394a90a85bf", "dosage_form": "TABLET, ORALLY DISINTEGRATING", "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": "43598-550", "generic_name": "Lamotrigine", "labeler_name": "Dr. Reddys Laboratories Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Lamotrigine", "active_ingredients": [{"name": "LAMOTRIGINE", "strength": "25 mg/1"}], "application_number": "ANDA206382", "marketing_category": "ANDA", "marketing_start_date": "20160617", "listing_expiration_date": "20261231"}