Package 71335-0830-6

Brand: lamotrigine

Generic: lamotrigine
NDC Package

Package Facts

Identity

Package NDC 71335-0830-6
Digits Only 7133508306
Product NDC 71335-0830
Description

14 TABLET in 1 BOTTLE (71335-0830-6)

Marketing

Marketing Status
Marketed Since 2022-02-09
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": "8bfcaf0d-599d-40e3-b4d9-2897a0e026a3", "openfda": {"nui": ["N0000175753", "N0000008486", "N0000175751", "N0000187061", "N0000000191"], "unii": ["U3H27498KS"], "rxcui": ["198429"], "spl_set_id": ["812bc0d8-bb31-4fb1-9f4a-f8c17cbc769c"], "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": ["Bryant Ranch Prepack"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET in 1 BOTTLE (71335-0830-1)", "package_ndc": "71335-0830-1", "marketing_start_date": "20220209"}, {"sample": false, "description": "60 TABLET in 1 BOTTLE (71335-0830-2)", "package_ndc": "71335-0830-2", "marketing_start_date": "20220209"}, {"sample": false, "description": "90 TABLET in 1 BOTTLE (71335-0830-3)", "package_ndc": "71335-0830-3", "marketing_start_date": "20220209"}, {"sample": false, "description": "45 TABLET in 1 BOTTLE (71335-0830-4)", "package_ndc": "71335-0830-4", "marketing_start_date": "20220209"}, {"sample": false, "description": "180 TABLET in 1 BOTTLE (71335-0830-5)", "package_ndc": "71335-0830-5", "marketing_start_date": "20220209"}, {"sample": false, "description": "14 TABLET in 1 BOTTLE (71335-0830-6)", "package_ndc": "71335-0830-6", "marketing_start_date": "20220209"}], "brand_name": "Lamotrigine", "product_id": "71335-0830_8bfcaf0d-599d-40e3-b4d9-2897a0e026a3", "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": "71335-0830", "generic_name": "Lamotrigine", "labeler_name": "Bryant Ranch Prepack", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Lamotrigine", "active_ingredients": [{"name": "LAMOTRIGINE", "strength": "200 mg/1"}], "application_number": "ANDA090170", "marketing_category": "ANDA", "marketing_start_date": "20111101", "listing_expiration_date": "20261231"}