Package 72189-432-09

Brand: sumatriptan succinate

Generic: sumatriptan succinate
NDC Package

Package Facts

Identity

Package NDC 72189-432-09
Digits Only 7218943209
Product NDC 72189-432
Product ID 72189-432_2c4d7702-337b-5298-e063-6394a90a7f3b
Description

9 TABLET, FILM COATED in 1 BOTTLE (72189-432-09)

Marketing

Marketing Status
Marketed Since 2023-03-13
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": "2c4d7702-337b-5298-e063-6394a90a7f3b", "openfda": {"unii": ["J8BDZ68989"], "rxcui": ["315223"], "spl_set_id": ["f6c95873-576d-a1c2-e053-6294a90a3ff9"], "manufacturer_name": ["Direct_Rx"]}, "finished": true, "packaging": [{"sample": false, "description": "9 TABLET, FILM COATED in 1 BOTTLE (72189-432-09)", "package_ndc": "72189-432-09", "marketing_start_date": "20230313"}], "brand_name": "Sumatriptan Succinate", "product_id": "72189-432_2c4d7702-337b-5298-e063-6394a90a7f3b", "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": "72189-432", "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": "ANDA078295", "marketing_category": "ANDA", "marketing_start_date": "20230313", "listing_expiration_date": "20261231"}