Package 68071-3607-6

Brand: lamotrigine

Generic: lamotrigine
NDC Package

Package Facts

Identity

Package NDC 68071-3607-6
Digits Only 6807136076
Product NDC 68071-3607
Description

60 TABLET in 1 BOTTLE (68071-3607-6)

Marketing

Marketing Status
Marketed Since 2024-06-25
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": "1bbbeda6-9835-6c1c-e063-6294a90ad1ab", "openfda": {"nui": ["N0000175753", "N0000008486", "N0000175751", "N0000187061", "N0000000191"], "upc": ["0368071360769"], "unii": ["U3H27498KS"], "rxcui": ["198427"], "spl_set_id": ["1bbbe2a2-a9e8-8c13-e063-6394a90a9627"], "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": ["NuCare Pharmaceuticals,Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "60 TABLET in 1 BOTTLE (68071-3607-6)", "package_ndc": "68071-3607-6", "marketing_start_date": "20240625"}], "brand_name": "LAMOTRIGINE", "product_id": "68071-3607_1bbbeda6-9835-6c1c-e063-6294a90ad1ab", "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": "68071-3607", "generic_name": "LAMOTRIGINE", "labeler_name": "NuCare Pharmaceuticals,Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "LAMOTRIGINE", "active_ingredients": [{"name": "LAMOTRIGINE", "strength": "100 mg/1"}], "application_number": "ANDA078947", "marketing_category": "ANDA", "marketing_start_date": "20090127", "listing_expiration_date": "20261231"}