Package 71335-2071-4
Brand: lamotrigine
Generic: lamotriginePackage Facts
Identity
Package NDC
71335-2071-4
Digits Only
7133520714
Product NDC
71335-2071
Description
120 TABLET in 1 BOTTLE (71335-2071-4)
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": "578c32bb-d9d4-48a7-9b64-28991e1a5750", "openfda": {"nui": ["N0000175753", "N0000008486", "N0000175751", "N0000187061", "N0000000191"], "unii": ["U3H27498KS"], "rxcui": ["198428"], "spl_set_id": ["68a4dac2-5015-40c5-88ca-204098c3b288"], "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": ["Bryant Ranch Prepack"]}, "finished": true, "packaging": [{"sample": false, "description": "60 TABLET in 1 BOTTLE (71335-2071-1)", "package_ndc": "71335-2071-1", "marketing_start_date": "20240403"}, {"sample": false, "description": "30 TABLET in 1 BOTTLE (71335-2071-2)", "package_ndc": "71335-2071-2", "marketing_start_date": "20220325"}, {"sample": false, "description": "90 TABLET in 1 BOTTLE (71335-2071-3)", "package_ndc": "71335-2071-3", "marketing_start_date": "20240403"}, {"sample": false, "description": "120 TABLET in 1 BOTTLE (71335-2071-4)", "package_ndc": "71335-2071-4", "marketing_start_date": "20240403"}, {"sample": false, "description": "180 TABLET in 1 BOTTLE (71335-2071-5)", "package_ndc": "71335-2071-5", "marketing_start_date": "20240403"}], "brand_name": "Lamotrigine", "product_id": "71335-2071_578c32bb-d9d4-48a7-9b64-28991e1a5750", "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": "71335-2071", "generic_name": "Lamotrigine", "labeler_name": "Bryant Ranch Prepack", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Lamotrigine", "active_ingredients": [{"name": "LAMOTRIGINE", "strength": "150 mg/1"}], "application_number": "ANDA078525", "marketing_category": "ANDA", "marketing_start_date": "20090127", "listing_expiration_date": "20261231"}