Package 51862-025-60

Brand: Dofetilide

Generic: Dofetilide
NDC Package

Package Facts

Identity

Package NDC 51862-025-60
Digits Only 5186202560
Product NDC 51862-025
Description

60 CAPSULE in 1 BOTTLE, PLASTIC (51862-025-60)

Marketing

Marketing Status
Discontinued 2026-02-28
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": "4a7bd9d4-6854-c23c-e063-6294a90a94de", "openfda": {"nui": ["N0000175426"], "upc": ["0351862025602"], "unii": ["R4Z9X1N2ND"], "spl_set_id": ["a806d3d2-d4c1-461c-b2e4-8807bfb59cb8"], "pharm_class_epc": ["Antiarrhythmic [EPC]"], "manufacturer_name": ["Mayne Pharma Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "60 CAPSULE in 1 BOTTLE, PLASTIC (51862-025-60)", "package_ndc": "51862-025-60", "marketing_end_date": "20260228", "marketing_start_date": "20160607"}], "brand_name": "Dofetilide", "product_id": "51862-025_4a7bd9d4-6854-c23c-e063-6294a90a94de", "dosage_form": "CAPSULE", "pharm_class": ["Antiarrhythmic [EPC]"], "product_ndc": "51862-025", "generic_name": "Dofetilide", "labeler_name": "Mayne Pharma Inc.", "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": "20260228", "marketing_start_date": "20160607"}