Package 72189-596-09

Brand: sumatriptan succinate

Generic: sumatriptan succinate
NDC Package

Package Facts

Identity

Package NDC 72189-596-09
Digits Only 7218959609
Product NDC 72189-596
Product ID 72189-596_284ee7ac-759f-b592-e063-6394a90a78ba
Description

9 TABLET, FILM COATED in 1 CARTON (72189-596-09)

Marketing

Marketing Status
Marketed Since 2024-12-02
Brand sumatriptan succinate
Generic sumatriptan succinate
Sample Package No

Linked Drug Pages (1)

Sumatriptan Succinate ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "284ee7ac-759f-b592-e063-6394a90a78ba", "openfda": {"unii": ["J8BDZ68989"], "rxcui": ["315223"], "spl_set_id": ["284ee7ac-759e-b592-e063-6394a90a78ba"], "manufacturer_name": ["Direct_Rx"]}, "finished": true, "packaging": [{"sample": false, "description": "9 TABLET, FILM COATED in 1 CARTON (72189-596-09)", "package_ndc": "72189-596-09", "marketing_start_date": "20241202"}], "brand_name": "Sumatriptan Succinate", "product_id": "72189-596_284ee7ac-759f-b592-e063-6394a90a78ba", "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": "72189-596", "generic_name": "Sumatriptan Succinate", "labeler_name": "Direct_Rx", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Sumatriptan Succinate", "active_ingredients": [{"name": "SUMATRIPTAN SUCCINATE", "strength": "25 mg/1"}], "application_number": "ANDA078284", "marketing_category": "ANDA", "marketing_start_date": "20241202", "listing_expiration_date": "20261231"}