Package 13668-266-28
Brand: lamotrigine
Generic: lamotriginePackage Facts
Identity
Package NDC
13668-266-28
Digits Only
1366826628
Product NDC
13668-266
Description
14 BLISTER PACK in 1 PACKAGE, COMBINATION (13668-266-28) / 1 KIT in 1 BLISTER PACK
Marketing
Marketing Status
Brand
lamotrigine
Generic
lamotrigine
Sample Package
No
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"spl_id": "e20d1c8d-dadf-4a54-8f0c-4ce62087f2e2", "openfda": {"nui": ["N0000175753", "N0000008486", "N0000175751", "N0000187061", "N0000000191"], "unii": ["U3H27498KS"], "rxcui": ["198427", "198428", "198429", "282401", "751139", "751563", "753451"], "spl_set_id": ["3448839b-4933-4ef9-a80a-9e504d2c5696"], "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": ["Torrent Pharmaceuticals Limited"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "14 BLISTER PACK in 1 PACKAGE, COMBINATION (13668-266-28) / 1 KIT in 1 BLISTER PACK", "package_ndc": "13668-266-28", "marketing_start_date": "20090127"}, {"sample": false, "description": "7 BLISTER PACK in 1 PACKAGE, COMBINATION (13668-266-99) / 1 KIT in 1 BLISTER PACK", "package_ndc": "13668-266-99", "marketing_start_date": "20090127"}], "brand_name": "LAMOTRIGINE", "product_id": "13668-266_e20d1c8d-dadf-4a54-8f0c-4ce62087f2e2", "dosage_form": "KIT", "product_ndc": "13668-266", "generic_name": "lamotrigine", "labeler_name": "Torrent Pharmaceuticals Limited", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "LAMOTRIGINE", "application_number": "ANDA078947", "marketing_category": "ANDA", "marketing_start_date": "20090127", "listing_expiration_date": "20271231"}