Package 65862-362-01

Brand: lamotrigine

Generic: lamotrigine
NDC Package

Package Facts

Identity

Package NDC 65862-362-01
Digits Only 6586236201
Product NDC 65862-362
Description

100 TABLET, CHEWABLE in 1 BOTTLE (65862-362-01)

Marketing

Marketing Status
Marketed Since 2009-11-04
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": "a1ae3fa7-d80d-42c3-bac5-5cccaee49ad7", "openfda": {"nui": ["N0000175753", "N0000008486", "N0000175751", "N0000187061", "N0000000191"], "upc": ["0365862361011"], "unii": ["U3H27498KS"], "rxcui": ["311264", "311265"], "spl_set_id": ["e08920c2-04a3-4fb5-acc5-0af3140f82e9"], "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": ["Aurobindo Pharma Limited"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET, CHEWABLE in 1 BOTTLE (65862-362-01)", "package_ndc": "65862-362-01", "marketing_start_date": "20091104"}, {"sample": false, "description": "500 TABLET, CHEWABLE in 1 BOTTLE (65862-362-05)", "package_ndc": "65862-362-05", "marketing_start_date": "20091104"}, {"sample": false, "description": "10 BLISTER PACK in 1 CARTON (65862-362-10)  / 10 TABLET, CHEWABLE in 1 BLISTER PACK", "package_ndc": "65862-362-10", "marketing_start_date": "20091104"}, {"sample": false, "description": "8000 TABLET, CHEWABLE in 1 BOTTLE (65862-362-81)", "package_ndc": "65862-362-81", "marketing_start_date": "20091104"}, {"sample": false, "description": "1000 TABLET, CHEWABLE in 1 BOTTLE (65862-362-99)", "package_ndc": "65862-362-99", "marketing_start_date": "20091104"}], "brand_name": "Lamotrigine", "product_id": "65862-362_a1ae3fa7-d80d-42c3-bac5-5cccaee49ad7", "dosage_form": "TABLET, CHEWABLE", "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": "65862-362", "generic_name": "Lamotrigine", "labeler_name": "Aurobindo Pharma Limited", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Lamotrigine", "active_ingredients": [{"name": "LAMOTRIGINE", "strength": "25 mg/1"}], "application_number": "ANDA090401", "marketing_category": "ANDA", "marketing_start_date": "20091104", "listing_expiration_date": "20261231"}