digoxin

Generic: digoxin

Labeler: northstar rx llc
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name digoxin
Generic Name digoxin
Labeler northstar rx llc
Dosage Form TABLET
Routes
ORAL
Active Ingredients

digoxin 125 ug/1

Manufacturer
Northstar Rx LLC

Identifiers & Regulatory

Product NDC 16714-590
Product ID 16714-590_9e663767-1f4a-4a9b-9571-fe7ba0ff10f5
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA076363
Marketing Start 2016-09-12
Marketing End 2026-04-30

Pharmacologic Class

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

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 16714590
Hyphenated Format 16714-590

Supplemental Identifiers

RxCUI
197604 197606
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 digoxin (source: ndc)
Generic Name digoxin (source: ndc)
Application Number ANDA076363 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 125 ug/1
source: ndc
Packaging
  • 1000 TABLET in 1 BOTTLE (16714-590-02)
source: ndc

Packages (1)

16714-590-02 1000 TABLET in 1 BOTTLE (16714-590-02)

Ingredients (1)

digoxin (125 ug/1)

Linked Drug Pages (1)

Digoxin ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "9e663767-1f4a-4a9b-9571-fe7ba0ff10f5", "openfda": {"nui": ["N0000175568", "M0003451"], "unii": ["73K4184T59"], "rxcui": ["197604", "197606"], "spl_set_id": ["8ec4abe0-7974-4921-b542-c9673dc5f77f"], "pharm_class_cs": ["Cardiac Glycosides [CS]"], "pharm_class_epc": ["Cardiac Glycoside [EPC]"], "manufacturer_name": ["Northstar Rx LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1000 TABLET in 1 BOTTLE (16714-590-02)", "package_ndc": "16714-590-02", "marketing_end_date": "20260430", "marketing_start_date": "20160912"}], "brand_name": "Digoxin", "product_id": "16714-590_9e663767-1f4a-4a9b-9571-fe7ba0ff10f5", "dosage_form": "TABLET", "pharm_class": ["Cardiac Glycoside [EPC]", "Cardiac Glycosides [CS]"], "product_ndc": "16714-590", "generic_name": "Digoxin", "labeler_name": "Northstar Rx LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Digoxin", "active_ingredients": [{"name": "DIGOXIN", "strength": "125 ug/1"}], "application_number": "ANDA076363", "marketing_category": "ANDA", "marketing_end_date": "20260430", "marketing_start_date": "20160912"}