Package 55111-226-30
Brand: lamotrigine
Generic: lamotriginePackage Facts
Identity
Package NDC
55111-226-30
Digits Only
5511122630
Product NDC
55111-226
Description
30 TABLET, CHEWABLE in 1 BOTTLE (55111-226-30)
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": "2cd813df-d72b-9337-d6ae-139b729a5e75", "openfda": {"nui": ["N0000175753", "N0000008486", "N0000175751", "N0000187061", "N0000000191"], "unii": ["U3H27498KS"], "rxcui": ["311264", "311265"], "spl_set_id": ["e1a0da17-d67c-e44f-bd42-33c4009e4cdd"], "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": "100 TABLET, CHEWABLE in 1 BOTTLE (55111-226-01)", "package_ndc": "55111-226-01", "marketing_start_date": "20090129"}, {"sample": false, "description": "500 TABLET, CHEWABLE in 1 BOTTLE (55111-226-05)", "package_ndc": "55111-226-05", "marketing_start_date": "20090129"}, {"sample": false, "description": "30 TABLET, CHEWABLE in 1 BOTTLE (55111-226-30)", "package_ndc": "55111-226-30", "marketing_start_date": "20090129"}, {"sample": false, "description": "60 TABLET, CHEWABLE in 1 BOTTLE (55111-226-60)", "package_ndc": "55111-226-60", "marketing_start_date": "20090129"}, {"sample": false, "description": "10 BLISTER PACK in 1 CARTON (55111-226-78) / 10 TABLET, CHEWABLE in 1 BLISTER PACK (55111-226-79)", "package_ndc": "55111-226-78", "marketing_start_date": "20090129"}], "brand_name": "Lamotrigine", "product_id": "55111-226_2cd813df-d72b-9337-d6ae-139b729a5e75", "dosage_form": "TABLET, CHEWABLE", "pharm_class": ["Anti-epileptic Agent [EPC]", "Decreased Central Nervous System Disorganized Electrical Activity [PE]", "Mood Stabilizer [EPC]"], "product_ndc": "55111-226", "generic_name": "Lamotrigine", "labeler_name": "Dr.Reddy's Laboratories Limited", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Lamotrigine", "active_ingredients": [{"name": "LAMOTRIGINE", "strength": "25 mg/1"}], "application_number": "ANDA076701", "marketing_category": "ANDA", "marketing_start_date": "20090129", "listing_expiration_date": "20261231"}