Package 0054-0279-03

Brand: naratriptan

Generic: naratriptan
NDC Package

Package Facts

Identity

Package NDC 0054-0279-03
Digits Only 0054027903
Product NDC 0054-0279
Description

9 TABLET in 1 BOTTLE (0054-0279-03)

Marketing

Marketing Status
Marketed Since 2010-10-07
Brand naratriptan
Generic naratriptan
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "14eeba7d-700d-4ac1-a71e-d6a1fca8aaab", "openfda": {"unii": ["10X8X4P12Z"], "rxcui": ["311918", "314135"], "spl_set_id": ["fd1944b3-8054-4faa-a82e-d818dfdd3875"], "manufacturer_name": ["Hikma Pharmaceuticals USA Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "9 TABLET in 1 BOTTLE (0054-0279-03)", "package_ndc": "0054-0279-03", "marketing_start_date": "20101007"}], "brand_name": "Naratriptan", "product_id": "0054-0279_14eeba7d-700d-4ac1-a71e-d6a1fca8aaab", "dosage_form": "TABLET", "pharm_class": ["Serotonin 1b Receptor Agonists [MoA]", "Serotonin 1d Receptor Agonists [MoA]", "Serotonin-1b and Serotonin-1d Receptor Agonist [EPC]"], "product_ndc": "0054-0279", "generic_name": "Naratriptan", "labeler_name": "Hikma Pharmaceuticals USA Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Naratriptan", "active_ingredients": [{"name": "NARATRIPTAN HYDROCHLORIDE", "strength": "2.5 mg/1"}], "application_number": "ANDA090381", "marketing_category": "ANDA", "marketing_start_date": "20100707", "listing_expiration_date": "20261231"}