Package 72189-433-09
Brand: sumatriptan succinate
Generic: sumatriptan succinatePackage Facts
Identity
Package NDC
72189-433-09
Digits Only
7218943309
Product NDC
72189-433
Description
9 TABLET, FILM COATED in 1 BOTTLE (72189-433-09)
Marketing
Marketing Status
Brand
sumatriptan succinate
Generic
sumatriptan succinate
Sample Package
No
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "2c4d7d0d-6552-336d-e063-6294a90a0ea4", "openfda": {"unii": ["J8BDZ68989"], "rxcui": ["313161"], "spl_set_id": ["f6c907a3-9624-f893-e053-6294a90a31af"], "manufacturer_name": ["Direct_Rx"]}, "finished": true, "packaging": [{"sample": false, "description": "9 TABLET, FILM COATED in 1 BOTTLE (72189-433-09)", "package_ndc": "72189-433-09", "marketing_start_date": "20230313"}], "brand_name": "Sumatriptan Succinate", "product_id": "72189-433_2c4d7d0d-6552-336d-e063-6294a90a0ea4", "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": "72189-433", "generic_name": "Sumatriptan Succinate", "labeler_name": "Direct_Rx", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Sumatriptan Succinate", "active_ingredients": [{"name": "SUMATRIPTAN SUCCINATE", "strength": "50 mg/1"}], "application_number": "ANDA078295", "marketing_category": "ANDA", "marketing_start_date": "20230313", "listing_expiration_date": "20261231"}