dofetilide
Generic: dofetilide
Labeler: bionpharma inc.Drug Facts
Product Profile
Brand Name
dofetilide
Generic Name
dofetilide
Labeler
bionpharma inc.
Dosage Form
CAPSULE
Routes
Active Ingredients
dofetilide .5 mg/1
Manufacturer
Identifiers & Regulatory
Product NDC
69452-133
Product ID
69452-133_f7811d48-6a19-d784-e053-6394a90aac27
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
ANDA
Application Number
ANDA208625
Listing Expiration
2026-12-31
Marketing Start
2018-04-11
Pharmacologic Class
Established (EPC)
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
69452133
Hyphenated Format
69452-133
Supplemental Identifiers
RxCUI
UPC
UNII
NUI
Packaging Origin
Original Packager
Resolved Product View
Precedence rule: structured NDC data is preferred, falling back to linked label metadata when unavailable. Source tags show the origin of each value.
Resolved Identity
Brand Name
dofetilide (source: ndc)
Generic Name
dofetilide (source: ndc)
Application Number
ANDA208625 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- .5 mg/1
Packaging
- 60 CAPSULE in 1 BOTTLE (69452-133-17)
Packages (1)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "f7811d48-6a19-d784-e053-6394a90aac27", "openfda": {"nui": ["N0000175426"], "upc": ["0369452133170", "0369452132173", "0369452131176"], "unii": ["R4Z9X1N2ND"], "rxcui": ["310003", "310004", "310005"], "spl_set_id": ["0e60aa4b-72c2-4ef4-ab01-c9cf94240ff1"], "pharm_class_epc": ["Antiarrhythmic [EPC]"], "manufacturer_name": ["Bionpharma Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "60 CAPSULE in 1 BOTTLE (69452-133-17)", "package_ndc": "69452-133-17", "marketing_start_date": "20180411"}], "brand_name": "Dofetilide", "product_id": "69452-133_f7811d48-6a19-d784-e053-6394a90aac27", "dosage_form": "CAPSULE", "pharm_class": ["Antiarrhythmic [EPC]"], "product_ndc": "69452-133", "generic_name": "Dofetilide", "labeler_name": "Bionpharma Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Dofetilide", "active_ingredients": [{"name": "DOFETILIDE", "strength": ".5 mg/1"}], "application_number": "ANDA208625", "marketing_category": "ANDA", "marketing_start_date": "20180411", "listing_expiration_date": "20261231"}