Package 72189-404-09

Brand: sumatriptan

Generic: sumatriptan
NDC Package

Package Facts

Identity

Package NDC 72189-404-09
Digits Only 7218940409
Product NDC 72189-404
Product ID 72189-404_2c4ce2c4-2b16-de10-e063-6394a90ad371
Description

9 TABLET, FILM COATED in 1 BOTTLE (72189-404-09)

Marketing

Marketing Status
Marketed Since 2022-12-13
Brand sumatriptan
Generic sumatriptan
Sample Package No

Linked Drug Pages (1)

Sumatriptan ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "2c4ce2c4-2b16-de10-e063-6394a90ad371", "openfda": {"unii": ["J8BDZ68989"], "rxcui": ["313160"], "spl_set_id": ["efb7ec4e-0a5d-2aae-e053-2a95a90aebf2"], "manufacturer_name": ["Direct_Rx"]}, "finished": true, "packaging": [{"sample": false, "description": "9 TABLET, FILM COATED in 1 BOTTLE (72189-404-09)", "package_ndc": "72189-404-09", "marketing_start_date": "20221213"}], "brand_name": "Sumatriptan", "product_id": "72189-404_2c4ce2c4-2b16-de10-e063-6394a90ad371", "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": "72189-404", "generic_name": "Sumatriptan", "labeler_name": "Direct_Rx", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Sumatriptan", "active_ingredients": [{"name": "SUMATRIPTAN SUCCINATE", "strength": "100 mg/1"}], "application_number": "ANDA078284", "marketing_category": "ANDA", "marketing_start_date": "20221213", "listing_expiration_date": "20261231"}