digoxin
Generic: digoxin
Labeler: proficient rx lpDrug Facts
Product Profile
Brand Name
digoxin
Generic Name
digoxin
Labeler
proficient rx lp
Dosage Form
TABLET
Routes
Active Ingredients
digoxin 250 ug/1
Manufacturer
Identifiers & Regulatory
Product NDC
82804-244
Product ID
82804-244_42d079a7-def1-4220-b71f-db2651966ffe
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
ANDA
Application Number
ANDA076268
Listing Expiration
2026-12-31
Marketing Start
2022-09-01
Pharmacologic Class
Established (EPC)
Chemical Structure
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
82804244
Hyphenated Format
82804-244
Supplemental Identifiers
RxCUI
UPC
UNII
NUI
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
digoxin (source: ndc)
Generic Name
digoxin (source: ndc)
Application Number
ANDA076268 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 250 ug/1
Packaging
- 90 TABLET in 1 BOTTLE (82804-244-90)
Packages (1)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "42d079a7-def1-4220-b71f-db2651966ffe", "openfda": {"nui": ["N0000175568", "M0003451"], "upc": ["0382804244904"], "unii": ["73K4184T59"], "rxcui": ["197606"], "spl_set_id": ["42d079a7-def1-4220-b71f-db2651966ffe"], "pharm_class_cs": ["Cardiac Glycosides [CS]"], "pharm_class_epc": ["Cardiac Glycoside [EPC]"], "manufacturer_name": ["Proficient Rx LP"]}, "finished": true, "packaging": [{"sample": false, "description": "90 TABLET in 1 BOTTLE (82804-244-90)", "package_ndc": "82804-244-90", "marketing_start_date": "20250915"}], "brand_name": "Digoxin", "product_id": "82804-244_42d079a7-def1-4220-b71f-db2651966ffe", "dosage_form": "TABLET", "pharm_class": ["Cardiac Glycoside [EPC]", "Cardiac Glycosides [CS]"], "product_ndc": "82804-244", "generic_name": "Digoxin", "labeler_name": "Proficient Rx LP", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Digoxin", "active_ingredients": [{"name": "DIGOXIN", "strength": "250 ug/1"}], "application_number": "ANDA076268", "marketing_category": "ANDA", "marketing_start_date": "20220901", "listing_expiration_date": "20261231"}