Package 76420-093-09

Brand: sumatriptan succinate

Generic: sumatriptan succinate
NDC Package

Package Facts

Identity

Package NDC 76420-093-09
Digits Only 7642009309
Product NDC 76420-093
Description

9 BLISTER PACK in 1 CARTON (76420-093-09) / 1 TABLET in 1 BLISTER PACK

Marketing

Marketing Status
Marketed Since 2020-10-24
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": "b26ec84b-1af1-b04d-e053-2a95a90a8c78", "openfda": {"unii": ["J8BDZ68989"], "rxcui": ["313161"], "spl_set_id": ["b16886d0-224b-4d83-85c4-bc3eb3606c17"], "manufacturer_name": ["Asclemed USA, Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "9 BLISTER PACK in 1 CARTON (76420-093-09)  / 1 TABLET in 1 BLISTER PACK", "package_ndc": "76420-093-09", "marketing_start_date": "20201024"}], "brand_name": "Sumatriptan Succinate", "product_id": "76420-093_b26ec84b-1af1-b04d-e053-2a95a90a8c78", "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": "76420-093", "generic_name": "Sumatriptan Succinate", "labeler_name": "Asclemed USA, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Sumatriptan Succinate", "active_ingredients": [{"name": "SUMATRIPTAN SUCCINATE", "strength": "50 mg/1"}], "application_number": "ANDA076847", "marketing_category": "ANDA", "marketing_start_date": "20091117", "listing_expiration_date": "20261231"}