Package 0904-7007-61

Brand: lamotrigine

Generic: lamotrigine
NDC Package

Package Facts

Identity

Package NDC 0904-7007-61
Digits Only 0904700761
Product NDC 0904-7007
Description

100 BLISTER PACK in 1 CARTON (0904-7007-61) / 1 TABLET in 1 BLISTER PACK

Marketing

Marketing Status
Marketed Since 2009-01-27
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": "587671e1-07fe-4e56-84f4-8a8ef59be0ba", "openfda": {"nui": ["N0000175753", "N0000008486", "N0000175751", "N0000187061", "N0000000191"], "unii": ["U3H27498KS"], "rxcui": ["198427", "282401"], "spl_set_id": ["12e0be85-0961-4fe0-b973-83251ecf0f65"], "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": ["Major Pharmaceuticals"]}, "finished": true, "packaging": [{"sample": false, "description": "100 BLISTER PACK in 1 CARTON (0904-7007-61)  / 1 TABLET in 1 BLISTER PACK", "package_ndc": "0904-7007-61", "marketing_start_date": "20090127"}], "brand_name": "Lamotrigine", "product_id": "0904-7007_587671e1-07fe-4e56-84f4-8a8ef59be0ba", "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": "0904-7007", "generic_name": "Lamotrigine", "labeler_name": "Major Pharmaceuticals", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Lamotrigine", "active_ingredients": [{"name": "LAMOTRIGINE", "strength": "25 mg/1"}], "application_number": "ANDA077633", "marketing_category": "ANDA", "marketing_start_date": "20090127", "listing_expiration_date": "20261231"}