Package 13668-049-13

Brand: lamotrigine

Generic: lamotrigine
NDC Package

Package Facts

Identity

Package NDC 13668-049-13
Digits Only 1366804913
Product NDC 13668-049
Description

1300 TABLET in 1 BOTTLE (13668-049-13)

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": "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": "100 TABLET in 1 BOTTLE (13668-049-01)", "package_ndc": "13668-049-01", "marketing_start_date": "20090127"}, {"sample": false, "description": "500 TABLET in 1 BOTTLE (13668-049-05)", "package_ndc": "13668-049-05", "marketing_start_date": "20090127"}, {"sample": false, "description": "1300 TABLET in 1 BOTTLE (13668-049-13)", "package_ndc": "13668-049-13", "marketing_start_date": "20090127"}, {"sample": false, "description": "30 TABLET in 1 BOTTLE (13668-049-30)", "package_ndc": "13668-049-30", "marketing_start_date": "20090127"}, {"sample": false, "description": "60 TABLET in 1 BOTTLE (13668-049-60)", "package_ndc": "13668-049-60", "marketing_start_date": "20090127"}, {"sample": false, "description": "90 TABLET in 1 DOSE PACK (13668-049-64)", "package_ndc": "13668-049-64", "marketing_start_date": "20090127"}], "brand_name": "LAMOTRIGINE", "product_id": "13668-049_e20d1c8d-dadf-4a54-8f0c-4ce62087f2e2", "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": "13668-049", "generic_name": "LAMOTRIGINE", "labeler_name": "Torrent Pharmaceuticals Limited", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "LAMOTRIGINE", "active_ingredients": [{"name": "LAMOTRIGINE", "strength": "200 mg/1"}], "application_number": "ANDA078947", "marketing_category": "ANDA", "marketing_start_date": "20090127", "listing_expiration_date": "20271231"}