digoxin

Generic: digoxin

Labeler: remedyrepack inc.
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name digoxin
Generic Name digoxin
Labeler remedyrepack inc.
Dosage Form TABLET
Routes
ORAL
Active Ingredients

digoxin .125 mg/1

Manufacturer
REMEDYREPACK INC.

Identifiers & Regulatory

Product NDC 70518-3859
Product ID 70518-3859_3f8ca510-9119-898d-e063-6394a90ad212
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA214982
Listing Expiration 2026-12-31
Marketing Start 2023-09-11

Pharmacologic Class

Established (EPC)
cardiac glycoside [epc]
Chemical Structure
cardiac glycosides [cs]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 705183859
Hyphenated Format 70518-3859

Supplemental Identifiers

RxCUI
197604
UNII
73K4184T59
NUI
N0000175568 M0003451

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 ANDA214982 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • .125 mg/1
source: ndc
Packaging
  • 30 TABLET in 1 BLISTER PACK (70518-3859-0)
source: ndc

Packages (1)

70518-3859-0 30 TABLET in 1 BLISTER PACK (70518-3859-0)

Ingredients (1)

digoxin (.125 mg/1)

Linked Drug Pages (1)

Digoxin ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "3f8ca510-9119-898d-e063-6394a90ad212", "openfda": {"nui": ["N0000175568", "M0003451"], "unii": ["73K4184T59"], "rxcui": ["197604"], "spl_set_id": ["dbc0bc24-f250-47e8-8d10-6aef551823d7"], "pharm_class_cs": ["Cardiac Glycosides [CS]"], "pharm_class_epc": ["Cardiac Glycoside [EPC]"], "manufacturer_name": ["REMEDYREPACK INC."]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET in 1 BLISTER PACK (70518-3859-0)", "package_ndc": "70518-3859-0", "marketing_start_date": "20230911"}], "brand_name": "Digoxin", "product_id": "70518-3859_3f8ca510-9119-898d-e063-6394a90ad212", "dosage_form": "TABLET", "pharm_class": ["Cardiac Glycoside [EPC]", "Cardiac Glycosides [CS]"], "product_ndc": "70518-3859", "generic_name": "Digoxin", "labeler_name": "REMEDYREPACK INC.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Digoxin", "active_ingredients": [{"name": "DIGOXIN", "strength": ".125 mg/1"}], "application_number": "ANDA214982", "marketing_category": "ANDA", "marketing_start_date": "20230911", "listing_expiration_date": "20261231"}