lanoxin
Generic: digoxin
Labeler: advanz pharma (us) corp.Drug Facts
Product Profile
Brand Name
lanoxin
Generic Name
digoxin
Labeler
advanz pharma (us) corp.
Dosage Form
TABLET
Routes
Active Ingredients
digoxin .125 mg/1
Manufacturer
Identifiers & Regulatory
Product NDC
59212-242
Product ID
59212-242_3a39029f-2e63-4894-8a0d-45e122f5047b
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
NDA
Application Number
NDA020405
Listing Expiration
2026-12-31
Marketing Start
2012-09-30
Pharmacologic Class
Established (EPC)
Chemical Structure
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
59212242
Hyphenated Format
59212-242
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
lanoxin (source: ndc)
Generic Name
digoxin (source: ndc)
Application Number
NDA020405 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- .125 mg/1
Packaging
- 100 TABLET in 1 BOTTLE (59212-242-55)
- 10 BLISTER PACK in 1 CARTON (59212-242-56) / 10 TABLET in 1 BLISTER PACK
Packages (2)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "3a39029f-2e63-4894-8a0d-45e122f5047b", "openfda": {"nui": ["N0000175568", "M0003451"], "upc": ["0359212240552", "0359212249555", "0359212242556"], "unii": ["73K4184T59"], "rxcui": ["104206", "197604", "197606", "245273", "309888", "309889", "1441565", "1441567"], "spl_set_id": ["d91e3646-4c63-4512-ab22-db39c085c4dc"], "pharm_class_cs": ["Cardiac Glycosides [CS]"], "pharm_class_epc": ["Cardiac Glycoside [EPC]"], "manufacturer_name": ["Advanz Pharma (US) Corp."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE (59212-242-55)", "package_ndc": "59212-242-55", "marketing_start_date": "20120930"}, {"sample": false, "description": "10 BLISTER PACK in 1 CARTON (59212-242-56) / 10 TABLET in 1 BLISTER PACK", "package_ndc": "59212-242-56", "marketing_start_date": "20120930"}], "brand_name": "LANOXIN", "product_id": "59212-242_3a39029f-2e63-4894-8a0d-45e122f5047b", "dosage_form": "TABLET", "pharm_class": ["Cardiac Glycoside [EPC]", "Cardiac Glycosides [CS]"], "product_ndc": "59212-242", "generic_name": "digoxin", "labeler_name": "Advanz Pharma (US) Corp.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "LANOXIN", "active_ingredients": [{"name": "DIGOXIN", "strength": ".125 mg/1"}], "application_number": "NDA020405", "marketing_category": "NDA", "marketing_start_date": "20120930", "listing_expiration_date": "20261231"}