Package 50090-7436-0

Brand: sumatriptan

Generic: sumatriptan
NDC Package

Package Facts

Identity

Package NDC 50090-7436-0
Digits Only 5009074360
Product NDC 50090-7436
Description

1 BLISTER PACK in 1 CARTON (50090-7436-0) / 9 TABLET, FILM COATED in 1 BLISTER PACK

Marketing

Marketing Status
Marketed Since 2024-11-06
Brand sumatriptan
Generic sumatriptan
Sample Package No

Linked Drug Pages (0)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "6a1a0b16-097b-47c2-aa32-01916f7df946", "openfda": {"unii": ["J8BDZ68989"], "rxcui": ["315223"], "spl_set_id": ["790acc89-81b3-4869-92e7-dc9f7fa6567b"], "manufacturer_name": ["A-S Medication Solutions"]}, "finished": true, "packaging": [{"sample": false, "description": "1 BLISTER PACK in 1 CARTON (50090-7436-0)  / 9 TABLET, FILM COATED in 1 BLISTER PACK", "package_ndc": "50090-7436-0", "marketing_start_date": "20241106"}], "brand_name": "Sumatriptan", "product_id": "50090-7436_6a1a0b16-097b-47c2-aa32-01916f7df946", "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": "50090-7436", "generic_name": "Sumatriptan", "labeler_name": "A-S Medication Solutions", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Sumatriptan", "active_ingredients": [{"name": "SUMATRIPTAN SUCCINATE", "strength": "25 mg/1"}], "application_number": "ANDA078284", "marketing_category": "ANDA", "marketing_start_date": "20220218", "listing_expiration_date": "20261231"}