Package 72189-560-30

Brand: lamotrigine er

Generic: lamotrigine er
NDC Package

Package Facts

Identity

Package NDC 72189-560-30
Digits Only 7218956030
Product NDC 72189-560
Description

30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (72189-560-30)

Marketing

Marketing Status
Marketed Since 2024-06-19
Brand lamotrigine er
Generic lamotrigine er
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "1b42a7cf-86d9-e506-e063-6394a90a3c9b", "openfda": {"nui": ["N0000175753", "N0000008486", "N0000175751", "N0000187061", "N0000000191"], "unii": ["U3H27498KS"], "rxcui": ["900156"], "spl_set_id": ["1b42a7cf-86d8-e506-e063-6394a90a3c9b"], "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": ["Direct_rx"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (72189-560-30)", "package_ndc": "72189-560-30", "marketing_start_date": "20240619"}], "brand_name": "Lamotrigine ER", "product_id": "72189-560_1b42a7cf-86d9-e506-e063-6394a90a3c9b", "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": "72189-560", "generic_name": "Lamotrigine ER", "labeler_name": "Direct_rx", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Lamotrigine ER", "active_ingredients": [{"name": "LAMOTRIGINE", "strength": "200 mg/1"}], "application_number": "ANDA213949", "marketing_category": "ANDA", "marketing_start_date": "20240619", "listing_expiration_date": "20261231"}