Package 68788-8619-9

Brand: sumatriptan

Generic: sumatriptan
NDC Package

Package Facts

Identity

Package NDC 68788-8619-9
Digits Only 6878886199
Product NDC 68788-8619
Description

1 BLISTER PACK in 1 CARTON (68788-8619-9) / 9 TABLET, FILM COATED in 1 BLISTER PACK

Marketing

Marketing Status
Marketed Since 2024-03-29
Brand sumatriptan
Generic sumatriptan
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "1820b836-cefb-418b-8d80-e387f2c289d8", "openfda": {"unii": ["J8BDZ68989"], "rxcui": ["313161"], "spl_set_id": ["0b9a0ab5-d8bd-4cae-b86c-45740ee1015a"], "manufacturer_name": ["Preferred Pharmaceuticals Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "1 BLISTER PACK in 1 CARTON (68788-8619-9)  / 9 TABLET, FILM COATED in 1 BLISTER PACK", "package_ndc": "68788-8619-9", "marketing_start_date": "20240329"}], "brand_name": "Sumatriptan", "product_id": "68788-8619_1820b836-cefb-418b-8d80-e387f2c289d8", "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": "68788-8619", "generic_name": "Sumatriptan", "labeler_name": "Preferred Pharmaceuticals Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Sumatriptan", "active_ingredients": [{"name": "SUMATRIPTAN SUCCINATE", "strength": "50 mg/1"}], "application_number": "ANDA078284", "marketing_category": "ANDA", "marketing_start_date": "20240329", "listing_expiration_date": "20261231"}