Package 76282-756-60

Brand: dofetilide

Generic: dofetilide
NDC Package

Package Facts

Identity

Package NDC 76282-756-60
Digits Only 7628275660
Product NDC 76282-756
Description

60 CAPSULE in 1 BOTTLE (76282-756-60)

Marketing

Marketing Status
Marketed Since 2024-11-01
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": "19f2a722-24ef-44f2-90e6-ec8df457baf6", "openfda": {"nui": ["N0000175426"], "upc": ["0376282756608", "0376282757605"], "unii": ["R4Z9X1N2ND"], "rxcui": ["310003", "310004", "310005"], "spl_set_id": ["41ccbb23-ae03-44bd-b438-0b0a8388d56b"], "pharm_class_epc": ["Antiarrhythmic [EPC]"], "manufacturer_name": ["EXELAN PHARMACEUTICALS, INC."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "60 CAPSULE in 1 BOTTLE (76282-756-60)", "package_ndc": "76282-756-60", "marketing_start_date": "20241101"}], "brand_name": "Dofetilide", "product_id": "76282-756_19f2a722-24ef-44f2-90e6-ec8df457baf6", "dosage_form": "CAPSULE", "pharm_class": ["Antiarrhythmic [EPC]"], "product_ndc": "76282-756", "generic_name": "Dofetilide", "labeler_name": "EXELAN PHARMACEUTICALS, INC.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Dofetilide", "active_ingredients": [{"name": "DOFETILIDE", "strength": ".25 mg/1"}], "application_number": "ANDA212750", "marketing_category": "ANDA", "marketing_start_date": "20241101", "listing_expiration_date": "20261231"}