lanoxin

Generic: digoxin

Labeler: advanz pharma (us) corp.
NDC Directory HUMAN PRESCRIPTION DRUG NDA Inactive Finished

Drug Facts

Product Profile

Brand Name lanoxin
Generic Name digoxin
Labeler advanz pharma (us) corp.
Dosage Form TABLET
Routes
ORAL
Active Ingredients

digoxin .125 mg/1

Manufacturer
Advanz Pharma (US) Corp.

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)
cardiac glycoside [epc]
Chemical Structure
cardiac glycosides [cs]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 59212242
Hyphenated Format 59212-242

Supplemental Identifiers

RxCUI
104206 197604 197606 245273 309888 309889 1441565 1441567
UPC
0359212240552 0359212249555 0359212242556
UNII
73K4184T59
NUI
N0000175568 M0003451

Packaging Origin

Original Packager
true

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
ORAL
source: ndc

Resolved Composition

Strengths
  • .125 mg/1
source: ndc
Packaging
  • 100 TABLET in 1 BOTTLE (59212-242-55)
  • 10 BLISTER PACK in 1 CARTON (59212-242-56) / 10 TABLET in 1 BLISTER PACK
source: ndc

Packages (2)

Ingredients (1)

digoxin (.125 mg/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"}