Package 49884-882-99

Brand: lamotrigine

Generic: lamotrigine
NDC Package

Package Facts

Identity

Package NDC 49884-882-99
Digits Only 4988488299
Product NDC 49884-882
Product ID 49884-882_9bb82767-a8f0-4956-875f-3d89731e1049
Description

1 BLISTER PACK in 1 PACKAGE, COMBINATION (49884-882-99) / 1 KIT in 1 BLISTER PACK

Marketing

Marketing Status
Marketed Since 2015-12-16
Brand lamotrigine
Generic lamotrigine
Sample Package No

Linked Drug Pages (1)

Lamotrigine ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"spl_id": "9bb82767-a8f0-4956-875f-3d89731e1049", "openfda": {"nui": ["N0000175753", "N0000008486", "N0000175751", "N0000187061", "N0000000191"], "unii": ["U3H27498KS"], "rxcui": ["103968", "198430", "252478", "252479", "851748", "851750", "851752"], "spl_set_id": ["003663e5-c0c7-4fc1-a64d-313f2a5b10d2"], "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": ["Endo USA, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 BLISTER PACK in 1 PACKAGE, COMBINATION (49884-882-99)  / 1 KIT in 1 BLISTER PACK", "package_ndc": "49884-882-99", "marketing_start_date": "20151216"}], "brand_name": "Lamotrigine", "product_id": "49884-882_9bb82767-a8f0-4956-875f-3d89731e1049", "dosage_form": "KIT", "product_ndc": "49884-882", "generic_name": "Lamotrigine", "labeler_name": "Endo USA, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Lamotrigine", "application_number": "ANDA204158", "marketing_category": "ANDA", "marketing_start_date": "20151127", "listing_expiration_date": "20261231"}