Package 71335-1469-1
Brand: lamotrigine
Generic: lamotriginePackage Facts
Identity
Package NDC
71335-1469-1
Digits Only
7133514691
Product NDC
71335-1469
Description
30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (71335-1469-1)
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": "917573a6-61bf-4b9c-8eba-cc4c79935072", "openfda": {"nui": ["N0000175753", "N0000008486", "N0000175751", "N0000187061", "N0000000191"], "unii": ["U3H27498KS"], "rxcui": ["900164"], "spl_set_id": ["36f383af-8b71-4875-85ef-3a7a8b1d8805"], "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": "30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (71335-1469-1)", "package_ndc": "71335-1469-1", "marketing_start_date": "20200110"}], "brand_name": "Lamotrigine", "product_id": "71335-1469_917573a6-61bf-4b9c-8eba-cc4c79935072", "dosage_form": "TABLET, FILM COATED, EXTENDED RELEASE", "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": "71335-1469", "generic_name": "Lamotrigine", "labeler_name": "Bryant Ranch Prepack", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Lamotrigine", "active_ingredients": [{"name": "LAMOTRIGINE", "strength": "25 mg/1"}], "application_number": "ANDA200672", "marketing_category": "ANDA", "marketing_start_date": "20160401", "listing_expiration_date": "20261231"}