Package 50228-321-30

Brand: lamotrigine

Generic: lamotrigine
NDC Package

Package Facts

Identity

Package NDC 50228-321-30
Digits Only 5022832130
Product NDC 50228-321
Description

30 TABLET, ORALLY DISINTEGRATING in 1 BOTTLE (50228-321-30)

Marketing

Marketing Status
Marketed Since 2015-11-30
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": "ec9440ec-0301-59bb-e053-2a95a90afe94", "openfda": {"nui": ["N0000175753", "N0000008486", "N0000175751", "N0000187061", "N0000000191"], "upc": ["0350228319300", "0350228320306", "0350228321303", "0350228322300"], "unii": ["U3H27498KS"], "rxcui": ["103968", "198430", "252478", "252479"], "spl_set_id": ["de700ac1-4048-467e-abb1-238953261a97"], "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": ["ScieGen Pharmaceuticals, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET, ORALLY DISINTEGRATING in 1 BOTTLE (50228-321-01)", "package_ndc": "50228-321-01", "marketing_start_date": "20151130"}, {"sample": false, "description": "30 TABLET, ORALLY DISINTEGRATING in 1 BOTTLE (50228-321-30)", "package_ndc": "50228-321-30", "marketing_start_date": "20151130"}], "brand_name": "Lamotrigine", "product_id": "50228-321_ec9440ec-0301-59bb-e053-2a95a90afe94", "dosage_form": "TABLET, ORALLY DISINTEGRATING", "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": "50228-321", "generic_name": "Lamotrigine", "labeler_name": "ScieGen Pharmaceuticals, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Lamotrigine", "active_ingredients": [{"name": "LAMOTRIGINE", "strength": "100 mg/1"}], "application_number": "ANDA206382", "marketing_category": "ANDA", "marketing_start_date": "20151130", "listing_expiration_date": "20261231"}