Package 42291-445-30

Brand: lamotrigine

Generic: lamotrigine
NDC Package

Package Facts

Identity

Package NDC 42291-445-30
Digits Only 4229144530
Product NDC 42291-445
Description

30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (42291-445-30)

Marketing

Marketing Status
Marketed Since 2020-05-22
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": "485d3fe4-eadb-a4dc-e063-6294a90ab9f0", "openfda": {"nui": ["N0000175753", "N0000008486", "N0000175751", "N0000187061", "N0000000191"], "unii": ["U3H27498KS"], "rxcui": ["850087", "850091", "900156", "900164", "1098608", "1146690"], "spl_set_id": ["a63e19c0-a093-e896-e053-2a95a90a7ccd"], "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": ["AvKARE"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (42291-445-30)", "package_ndc": "42291-445-30", "marketing_start_date": "20200522"}], "brand_name": "Lamotrigine", "product_id": "42291-445_485d3fe4-eadb-a4dc-e063-6294a90ab9f0", "dosage_form": "TABLET, FILM COATED, EXTENDED RELEASE", "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": "42291-445", "generic_name": "Lamotrigine", "labeler_name": "AvKARE", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Lamotrigine", "active_ingredients": [{"name": "LAMOTRIGINE", "strength": "100 mg/1"}], "application_number": "ANDA207497", "marketing_category": "ANDA", "marketing_start_date": "20200522", "listing_expiration_date": "20271231"}