Package 0904-6682-08

Brand: Dofetilide

Generic: Dofetilide
NDC Package

Package Facts

Identity

Package NDC 0904-6682-08
Digits Only 0904668208
Product NDC 0904-6682
Product ID 0904-6682_10308f39-43be-45ec-ab9c-a05973ffea21
Description

40 BLISTER PACK in 1 CARTON (0904-6682-08) / 1 CAPSULE in 1 BLISTER PACK

Marketing

Marketing Status
Discontinued 2026-03-31
Brand Dofetilide
Generic Dofetilide
Sample Package No

Linked Drug Pages (1)

Dofetilide ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "10308f39-43be-45ec-ab9c-a05973ffea21", "openfda": {"nui": ["N0000175426"], "unii": ["R4Z9X1N2ND"], "rxcui": ["310003", "310004", "310005"], "spl_set_id": ["878263a5-b2a1-4aa0-84cc-7fc165ee86c9"], "pharm_class_epc": ["Antiarrhythmic [EPC]"], "manufacturer_name": ["Major Pharmaceuticals"]}, "finished": true, "packaging": [{"sample": false, "description": "40 BLISTER PACK in 1 CARTON (0904-6682-08)  / 1 CAPSULE in 1 BLISTER PACK", "package_ndc": "0904-6682-08", "marketing_end_date": "20260331", "marketing_start_date": "20160607"}], "brand_name": "Dofetilide", "product_id": "0904-6682_10308f39-43be-45ec-ab9c-a05973ffea21", "dosage_form": "CAPSULE", "pharm_class": ["Antiarrhythmic [EPC]"], "product_ndc": "0904-6682", "generic_name": "Dofetilide", "labeler_name": "Major Pharmaceuticals", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Dofetilide", "active_ingredients": [{"name": "DOFETILIDE", "strength": ".25 mg/1"}], "application_number": "ANDA207058", "marketing_category": "ANDA", "marketing_end_date": "20260331", "marketing_start_date": "20160607"}