Package 72789-206-60
Brand: lamotrigine
Generic: lamotriginePackage Facts
Identity
Package NDC
72789-206-60
Digits Only
7278920660
Product NDC
72789-206
Description
60 TABLET in 1 BOTTLE, PLASTIC (72789-206-60)
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": "4b086cf2-a3b3-f59d-e063-6294a90abeb9", "openfda": {"nui": ["N0000175753", "N0000008486", "N0000175751", "N0000187061", "N0000000191"], "upc": ["0372789206608"], "unii": ["U3H27498KS"], "rxcui": ["198427"], "spl_set_id": ["dc6e6735-d49a-44d8-936d-7c33437bc59e"], "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": ["PD-Rx Pharmaceuticals, Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "60 TABLET in 1 BOTTLE, PLASTIC (72789-206-60)", "package_ndc": "72789-206-60", "marketing_start_date": "20210927"}], "brand_name": "Lamotrigine", "product_id": "72789-206_4b086cf2-a3b3-f59d-e063-6294a90abeb9", "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": "72789-206", "generic_name": "Lamotrigine", "labeler_name": "PD-Rx Pharmaceuticals, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Lamotrigine", "active_ingredients": [{"name": "LAMOTRIGINE", "strength": "100 mg/1"}], "application_number": "ANDA090170", "marketing_category": "ANDA", "marketing_start_date": "20111101", "listing_expiration_date": "20271231"}