Package 72603-131-01

Brand: dofetilide

Generic: dofetilide
NDC Package

Package Facts

Identity

Package NDC 72603-131-01
Digits Only 7260313101
Product NDC 72603-131
Description

60 CAPSULE in 1 BOTTLE (72603-131-01)

Marketing

Marketing Status
Marketed Since 2023-02-07
Brand dofetilide
Generic dofetilide
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "d9cc5e83-13c7-40a5-86d3-29216f7f55fe", "openfda": {"nui": ["N0000175426"], "upc": ["0372603130010", "0372603132014", "0372603131017"], "unii": ["R4Z9X1N2ND"], "rxcui": ["310003", "310004", "310005"], "spl_set_id": ["4552d82a-dd28-410c-9642-1af060832b47"], "pharm_class_epc": ["Antiarrhythmic [EPC]"], "manufacturer_name": ["NorthStar RxLLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "60 CAPSULE in 1 BOTTLE (72603-131-01)", "package_ndc": "72603-131-01", "marketing_start_date": "20230207"}], "brand_name": "DOFETILIDE", "product_id": "72603-131_d9cc5e83-13c7-40a5-86d3-29216f7f55fe", "dosage_form": "CAPSULE", "pharm_class": ["Antiarrhythmic [EPC]"], "product_ndc": "72603-131", "generic_name": "DOFETILIDE", "labeler_name": "NorthStar RxLLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "DOFETILIDE", "active_ingredients": [{"name": "DOFETILIDE", "strength": ".25 mg/1"}], "application_number": "ANDA210466", "marketing_category": "ANDA", "marketing_start_date": "20230207", "listing_expiration_date": "20261231"}