Package 0904-7522-08

Brand: dofetilide

Generic: dofetilide
NDC Package

Package Facts

Identity

Package NDC 0904-7522-08
Digits Only 0904752208
Product NDC 0904-7522
Product ID 0904-7522_163839ff-a9c4-428a-a920-65dd07532384
Description

40 BLISTER PACK in 1 CARTON (0904-7522-08) / 1 CAPSULE in 1 BLISTER PACK

Marketing

Marketing Status
Marketed Since 2024-10-17
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": "163839ff-a9c4-428a-a920-65dd07532384", "openfda": {"nui": ["N0000175426"], "unii": ["R4Z9X1N2ND"], "rxcui": ["310003", "310004", "310005"], "spl_set_id": ["26de5f8c-8cec-46f6-a468-69451758a278"], "pharm_class_epc": ["Antiarrhythmic [EPC]"], "manufacturer_name": ["Major Pharmaceuticals"]}, "finished": true, "packaging": [{"sample": false, "description": "40 BLISTER PACK in 1 CARTON (0904-7522-08)  / 1 CAPSULE in 1 BLISTER PACK", "package_ndc": "0904-7522-08", "marketing_start_date": "20241017"}], "brand_name": "Dofetilide", "product_id": "0904-7522_163839ff-a9c4-428a-a920-65dd07532384", "dosage_form": "CAPSULE", "pharm_class": ["Antiarrhythmic [EPC]"], "product_ndc": "0904-7522", "generic_name": "Dofetilide", "labeler_name": "Major Pharmaceuticals", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Dofetilide", "active_ingredients": [{"name": "DOFETILIDE", "strength": ".125 mg/1"}], "application_number": "ANDA207058", "marketing_category": "ANDA", "marketing_start_date": "20241017", "listing_expiration_date": "20261231"}