Package 76420-500-09

Brand: sumatriptan

Generic: sumatriptan succinate
NDC Package

Package Facts

Identity

Package NDC 76420-500-09
Digits Only 7642050009
Product NDC 76420-500
Product ID 76420-500_eacf382a-98ac-e3ad-e053-2995a90a44e8
Description

9 TABLET in 1 BLISTER PACK (76420-500-09)

Marketing

Marketing Status
Marketed Since 2022-10-12
Brand sumatriptan
Generic sumatriptan succinate
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": "eacf382a-98ac-e3ad-e053-2995a90a44e8", "openfda": {"unii": ["J8BDZ68989"], "rxcui": ["313160", "313161", "315223"], "spl_set_id": ["77f9f135-e840-48f0-81e8-73e08433e768"], "manufacturer_name": ["Asclemed USA, Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "9 TABLET in 1 BLISTER PACK (76420-500-09)", "package_ndc": "76420-500-09", "marketing_start_date": "20221012"}], "brand_name": "Sumatriptan", "product_id": "76420-500_eacf382a-98ac-e3ad-e053-2995a90a44e8", "dosage_form": "TABLET", "pharm_class": ["Serotonin 1b Receptor Agonists [MoA]", "Serotonin 1d Receptor Agonists [MoA]", "Serotonin-1b and Serotonin-1d Receptor Agonist [EPC]"], "product_ndc": "76420-500", "generic_name": "Sumatriptan Succinate", "labeler_name": "Asclemed USA, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Sumatriptan", "active_ingredients": [{"name": "SUMATRIPTAN SUCCINATE", "strength": "100 mg/1"}], "application_number": "ANDA078327", "marketing_category": "ANDA", "marketing_start_date": "20090817", "listing_expiration_date": "20261231"}