Package 29300-112-10

Brand: lamotrigine

Generic: lamotrigine
NDC Package

Package Facts

Identity

Package NDC 29300-112-10
Digits Only 2930011210
Product NDC 29300-112
Description

1000 TABLET in 1 BOTTLE, PLASTIC (29300-112-10)

Marketing

Marketing Status
Marketed Since 2011-11-01
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": "03f59daf-b60e-46d1-b121-6a39361ee4f3", "openfda": {"nui": ["N0000175753", "N0000008486", "N0000175751", "N0000187061", "N0000000191"], "upc": ["0329300113167", "0329300111019", "0329300114164"], "unii": ["U3H27498KS"], "rxcui": ["198427", "198428", "198429", "282401"], "spl_set_id": ["4b72ea7a-a0b0-4980-84ad-84f64e2e6368"], "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": ["Unichem Pharmaceuticals (USA), Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE, PLASTIC (29300-112-01)", "package_ndc": "29300-112-01", "marketing_start_date": "20111101"}, {"sample": false, "description": "500 TABLET in 1 BOTTLE, PLASTIC (29300-112-05)", "package_ndc": "29300-112-05", "marketing_start_date": "20111101"}, {"sample": false, "description": "1000 TABLET in 1 BOTTLE, PLASTIC (29300-112-10)", "package_ndc": "29300-112-10", "marketing_start_date": "20111101"}], "brand_name": "Lamotrigine", "product_id": "29300-112_03f59daf-b60e-46d1-b121-6a39361ee4f3", "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": "29300-112", "generic_name": "Lamotrigine", "labeler_name": "Unichem Pharmaceuticals (USA), Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Lamotrigine", "active_ingredients": [{"name": "LAMOTRIGINE", "strength": "100 mg/1"}], "application_number": "ANDA090170", "marketing_category": "ANDA", "marketing_start_date": "20111101", "listing_expiration_date": "20261231"}