Package 68382-009-14

Brand: lamotrigine

Generic: lamotrigine
NDC Package

Package Facts

Identity

Package NDC 68382-009-14
Digits Only 6838200914
Product NDC 68382-009
Description

60 TABLET in 1 BOTTLE (68382-009-14)

Marketing

Marketing Status
Marketed Since 2009-01-27
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": "277200d5-a863-4411-8c1b-aac8d7fde6a6", "openfda": {"nui": ["N0000175753", "N0000008486", "N0000175751", "N0000187061", "N0000000191"], "upc": ["0368382109019", "0368382011053", "0368382108012"], "unii": ["U3H27498KS"], "rxcui": ["198427", "198428", "198429", "199322", "249329", "282401", "311264", "311265"], "spl_set_id": ["e849033b-a3bc-408e-88de-7cd1d2660949"], "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": ["Zydus Pharmaceuticals USA Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "500 TABLET in 1 BOTTLE (68382-009-05)", "package_ndc": "68382-009-05", "marketing_start_date": "20090127"}, {"sample": false, "description": "60 TABLET in 1 BOTTLE (68382-009-14)", "package_ndc": "68382-009-14", "marketing_start_date": "20090127"}, {"sample": false, "description": "90 TABLET in 1 BOTTLE (68382-009-16)", "package_ndc": "68382-009-16", "marketing_start_date": "20090127"}], "brand_name": "Lamotrigine", "product_id": "68382-009_277200d5-a863-4411-8c1b-aac8d7fde6a6", "dosage_form": "TABLET", "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": "68382-009", "generic_name": "Lamotrigine", "labeler_name": "Zydus Pharmaceuticals USA Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Lamotrigine", "active_ingredients": [{"name": "LAMOTRIGINE", "strength": "150 mg/1"}], "application_number": "ANDA077633", "marketing_category": "ANDA", "marketing_start_date": "20090127", "listing_expiration_date": "20261231"}