Package 68462-228-90

Brand: lamotrigine

Generic: lamotrigine
NDC Package

Package Facts

Identity

Package NDC 68462-228-90
Digits Only 6846222890
Product NDC 68462-228
Description

90 TABLET, CHEWABLE in 1 BOTTLE (68462-228-90)

Marketing

Marketing Status
Marketed Since 2009-02-19
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": "fc701d94-bfc5-44c4-8667-6414ee7226ed", "openfda": {"nui": ["N0000175753", "N0000008486", "N0000175751", "N0000187061", "N0000000191"], "upc": ["0368462228012", "0368462229019"], "unii": ["U3H27498KS"], "rxcui": ["311264", "311265"], "spl_set_id": ["50fcf452-2d21-493e-a1dd-0c6ea9ac6184"], "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": ["Glenmark Pharmaceuticals Inc., USA"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET, CHEWABLE in 1 BOTTLE (68462-228-01)", "package_ndc": "68462-228-01", "marketing_start_date": "20090219"}, {"sample": false, "description": "1000 TABLET, CHEWABLE in 1 BOTTLE (68462-228-10)", "package_ndc": "68462-228-10", "marketing_start_date": "20090219"}, {"sample": false, "description": "90 TABLET, CHEWABLE in 1 BOTTLE (68462-228-90)", "package_ndc": "68462-228-90", "marketing_start_date": "20090219"}], "brand_name": "Lamotrigine", "product_id": "68462-228_fc701d94-bfc5-44c4-8667-6414ee7226ed", "dosage_form": "TABLET, CHEWABLE", "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": "68462-228", "generic_name": "Lamotrigine", "labeler_name": "Glenmark Pharmaceuticals Inc., USA", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Lamotrigine", "active_ingredients": [{"name": "LAMOTRIGINE", "strength": "5 mg/1"}], "application_number": "ANDA079099", "marketing_category": "ANDA", "marketing_start_date": "20090219", "listing_expiration_date": "20271231"}