Package 71205-111-01

Brand: sumatriptan succinate

Generic: sumatriptan succinate
NDC Package

Package Facts

Identity

Package NDC 71205-111-01
Digits Only 7120511101
Product NDC 71205-111
Description

1 mL in 1 VIAL (71205-111-01)

Marketing

Marketing Status
Marketed Since 2018-09-04
Brand sumatriptan succinate
Generic sumatriptan succinate
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["SUBCUTANEOUS"], "spl_id": "7fef2881-dce5-4746-85bc-edb02e8ea0c5", "openfda": {"unii": ["J8BDZ68989"], "rxcui": ["313165"], "spl_set_id": ["44d6d757-489c-4262-a518-af8c470734d6"], "manufacturer_name": ["Proficient Rx LP"]}, "finished": true, "packaging": [{"sample": false, "description": "1 mL in 1 VIAL (71205-111-01)", "package_ndc": "71205-111-01", "marketing_start_date": "20180904"}], "brand_name": "Sumatriptan Succinate", "product_id": "71205-111_7fef2881-dce5-4746-85bc-edb02e8ea0c5", "dosage_form": "INJECTION", "pharm_class": ["Serotonin 1b Receptor Agonists [MoA]", "Serotonin 1d Receptor Agonists [MoA]", "Serotonin-1b and Serotonin-1d Receptor Agonist [EPC]"], "product_ndc": "71205-111", "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": "6 mg/.5mL"}], "application_number": "ANDA078593", "marketing_category": "ANDA", "marketing_start_date": "20090206", "listing_expiration_date": "20261231"}