Package 68788-6769-9
Brand: sumatriptan
Generic: sumatriptan succinatePackage Facts
Identity
Package NDC
68788-6769-9
Digits Only
6878867699
Product NDC
68788-6769
Description
9 TABLET in 1 BLISTER PACK (68788-6769-9)
Marketing
Marketing Status
Brand
sumatriptan
Generic
sumatriptan succinate
Sample Package
No
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "d44ab3f6-b246-479c-906b-eb94f6549a1c", "openfda": {"unii": ["J8BDZ68989"], "rxcui": ["315223"], "spl_set_id": ["baf37e8c-d414-4ca7-a366-97dc202372ff"], "manufacturer_name": ["Preferred Pharmaceuticals Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "9 TABLET in 1 BLISTER PACK (68788-6769-9)", "package_ndc": "68788-6769-9", "marketing_start_date": "20161024"}], "brand_name": "Sumatriptan", "product_id": "68788-6769_d44ab3f6-b246-479c-906b-eb94f6549a1c", "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": "68788-6769", "generic_name": "Sumatriptan Succinate", "labeler_name": "Preferred Pharmaceuticals Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Sumatriptan", "active_ingredients": [{"name": "SUMATRIPTAN SUCCINATE", "strength": "25 mg/1"}], "application_number": "ANDA078327", "marketing_category": "ANDA", "marketing_start_date": "20161024", "listing_expiration_date": "20261231"}