Package 65841-686-05
Brand: lamotrigine
Generic: lamotriginePackage Facts
Identity
Package NDC
65841-686-05
Digits Only
6584168605
Product NDC
65841-686
Description
500 TABLET in 1 BOTTLE (65841-686-05)
Marketing
Marketing Status
Brand
lamotrigine
Generic
lamotrigine
Sample Package
No
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "c4eb074b-9cd4-4bcd-868c-473d9364061c", "openfda": {"nui": ["N0000175753", "N0000008486", "N0000175751", "N0000187061", "N0000000191"], "upc": ["0365841687057"], "unii": ["U3H27498KS"], "rxcui": ["198427", "198428", "198429", "199322", "249329", "282401", "311264", "311265"], "spl_set_id": ["0f2f7421-56d4-45d0-9d2d-dc1edaede039"], "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": ["Zydus Lifesciences Limited"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "500 TABLET in 1 BOTTLE (65841-686-05)", "package_ndc": "65841-686-05", "marketing_start_date": "20090127"}, {"sample": false, "description": "60 TABLET in 1 BOTTLE (65841-686-14)", "package_ndc": "65841-686-14", "marketing_start_date": "20090127"}, {"sample": false, "description": "90 TABLET in 1 BOTTLE (65841-686-16)", "package_ndc": "65841-686-16", "marketing_start_date": "20090127"}], "brand_name": "Lamotrigine", "product_id": "65841-686_c4eb074b-9cd4-4bcd-868c-473d9364061c", "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": "65841-686", "generic_name": "Lamotrigine", "labeler_name": "Zydus Lifesciences Limited", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Lamotrigine", "active_ingredients": [{"name": "LAMOTRIGINE", "strength": "200 mg/1"}], "application_number": "ANDA077633", "marketing_category": "ANDA", "marketing_start_date": "20090127", "listing_expiration_date": "20261231"}