Package 60687-704-01
Brand: lamotrigine
Generic: lamotriginePackage Facts
Identity
Package NDC
60687-704-01
Digits Only
6068770401
Product NDC
60687-704
Description
100 BLISTER PACK in 1 CARTON (60687-704-01) / 1 TABLET in 1 BLISTER PACK (60687-704-11)
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": "4c0eeb34-9d52-f6e8-e063-6294a90a4eff", "openfda": {"nui": ["N0000175753", "N0000008486", "N0000175751", "N0000187061", "N0000000191"], "unii": ["U3H27498KS"], "rxcui": ["198428", "198429"], "spl_set_id": ["6034a8b8-9e80-43ca-b84f-ea82f788268c"], "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": ["American Health Packaging"]}, "finished": true, "packaging": [{"sample": false, "description": "100 BLISTER PACK in 1 CARTON (60687-704-01) / 1 TABLET in 1 BLISTER PACK (60687-704-11)", "package_ndc": "60687-704-01", "marketing_start_date": "20230117"}], "brand_name": "Lamotrigine", "product_id": "60687-704_4c0eeb34-9d52-f6e8-e063-6294a90a4eff", "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": "60687-704", "generic_name": "Lamotrigine", "labeler_name": "American Health Packaging", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Lamotrigine", "active_ingredients": [{"name": "LAMOTRIGINE", "strength": "200 mg/1"}], "application_number": "ANDA077633", "marketing_category": "ANDA", "marketing_start_date": "20230117", "listing_expiration_date": "20271231"}