Package 80425-0475-1

Brand: sumatriptan

Generic: sumatriptan
NDC Package

Package Facts

Identity

Package NDC 80425-0475-1
Digits Only 8042504751
Product NDC 80425-0475
Description

1 BLISTER PACK in 1 CARTON (80425-0475-1) / 9 TABLET, FILM COATED in 1 BLISTER PACK

Marketing

Marketing Status
Marketed Since 2024-12-30
Brand sumatriptan
Generic sumatriptan
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "2aab828f-48fd-5ff9-e063-6394a90ac966", "openfda": {"unii": ["J8BDZ68989"], "rxcui": ["313161"], "spl_set_id": ["2aab8786-b225-833a-e063-6394a90ac7ae"], "manufacturer_name": ["Advanced Rx of Tennessee, LLC"]}, "finished": true, "packaging": [{"sample": false, "description": "1 BLISTER PACK in 1 CARTON (80425-0475-1)  / 9 TABLET, FILM COATED in 1 BLISTER PACK", "package_ndc": "80425-0475-1", "marketing_start_date": "20241230"}], "brand_name": "Sumatriptan", "product_id": "80425-0475_2aab828f-48fd-5ff9-e063-6394a90ac966", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Serotonin 1b Receptor Agonists [MoA]", "Serotonin 1d Receptor Agonists [MoA]", "Serotonin-1b and Serotonin-1d Receptor Agonist [EPC]"], "product_ndc": "80425-0475", "generic_name": "Sumatriptan", "labeler_name": "Advanced Rx of Tennessee, LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Sumatriptan", "active_ingredients": [{"name": "SUMATRIPTAN SUCCINATE", "strength": "50 mg/1"}], "application_number": "ANDA078284", "marketing_category": "ANDA", "marketing_start_date": "20241230", "listing_expiration_date": "20261231"}