Package 63187-049-09

Brand: sumatriptan succinate

Generic: sumatriptan succinate
NDC Package

Package Facts

Identity

Package NDC 63187-049-09
Digits Only 6318704909
Product NDC 63187-049
Description

9 TABLET in 1 BOTTLE (63187-049-09)

Marketing

Marketing Status
Marketed Since 2014-05-01
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": "bcf1b59f-5656-4913-882c-95ffe205273b", "openfda": {"unii": ["J8BDZ68989"], "rxcui": ["313161"], "spl_set_id": ["68daf82a-334e-43ca-b4bb-5c66a82f52c8"], "manufacturer_name": ["Proficient Rx LP"]}, "finished": true, "packaging": [{"sample": false, "description": "9 TABLET in 1 BOTTLE (63187-049-09)", "package_ndc": "63187-049-09", "marketing_start_date": "20140501"}], "brand_name": "Sumatriptan Succinate", "product_id": "63187-049_bcf1b59f-5656-4913-882c-95ffe205273b", "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": "63187-049", "generic_name": "Sumatriptan Succinate", "labeler_name": "Proficient Rx LP", "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"}