Package 55111-428-05
Brand: lamotrigine
Generic: lamotriginePackage Facts
Identity
Package NDC
55111-428-05
Digits Only
5511142805
Product NDC
55111-428
Description
500 TABLET, EXTENDED RELEASE in 1 BOTTLE (55111-428-05)
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": "236437dc-fce9-b140-992c-b7822562eee5", "openfda": {"nui": ["N0000175753", "N0000008486", "N0000175751", "N0000187061", "N0000000191"], "unii": ["U3H27498KS"], "rxcui": ["850087", "850091", "900156", "900164", "1098608", "1146690"], "spl_set_id": ["a69542ea-5b6f-15c1-9e7a-90ac839971d3"], "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": ["Dr.Reddy's Laboratories Limited"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "500 TABLET, EXTENDED RELEASE in 1 BOTTLE (55111-428-05)", "package_ndc": "55111-428-05", "marketing_start_date": "20130620"}, {"sample": false, "description": "30 TABLET, EXTENDED RELEASE in 1 BOTTLE (55111-428-30)", "package_ndc": "55111-428-30", "marketing_start_date": "20130620"}, {"sample": false, "description": "90 TABLET, EXTENDED RELEASE in 1 BOTTLE (55111-428-90)", "package_ndc": "55111-428-90", "marketing_start_date": "20130620"}], "brand_name": "Lamotrigine", "product_id": "55111-428_236437dc-fce9-b140-992c-b7822562eee5", "dosage_form": "TABLET, 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": "55111-428", "generic_name": "Lamotrigine", "labeler_name": "Dr.Reddy's Laboratories Limited", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Lamotrigine", "active_ingredients": [{"name": "LAMOTRIGINE", "strength": "300 mg/1"}], "application_number": "ANDA202383", "marketing_category": "ANDA", "marketing_start_date": "20130620", "listing_expiration_date": "20271231"}