digoxin

Generic: digoxin

Labeler: bryant ranch prepack
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name digoxin
Generic Name digoxin
Labeler bryant ranch prepack
Dosage Form TABLET
Routes
ORAL
Active Ingredients

digoxin 125 ug/1

Manufacturer
Bryant Ranch Prepack

Identifiers & Regulatory

Product NDC 71335-9610
Product ID 71335-9610_0c658a0b-598c-4a44-a00a-7da9cb475f95
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA076363
Listing Expiration 2026-12-31
Marketing Start 2015-02-17

Pharmacologic Class

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

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 713359610
Hyphenated Format 71335-9610

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 ANDA076363 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 125 ug/1
source: ndc
Packaging
  • 30 TABLET in 1 BOTTLE (71335-9610-1)
  • 90 TABLET in 1 BOTTLE (71335-9610-2)
  • 15 TABLET in 1 BOTTLE (71335-9610-3)
  • 6 TABLET in 1 BOTTLE (71335-9610-4)
  • 60 TABLET in 1 BOTTLE (71335-9610-5)
  • 100 TABLET in 1 BOTTLE (71335-9610-6)
  • 10 TABLET in 1 BOTTLE (71335-9610-7)
source: ndc

Packages (7)

71335-9610-1 30 TABLET in 1 BOTTLE (71335-9610-1) 71335-9610-2 90 TABLET in 1 BOTTLE (71335-9610-2) 71335-9610-3 15 TABLET in 1 BOTTLE (71335-9610-3) 71335-9610-4 6 TABLET in 1 BOTTLE (71335-9610-4) 71335-9610-5 60 TABLET in 1 BOTTLE (71335-9610-5) 71335-9610-6 100 TABLET in 1 BOTTLE (71335-9610-6) 71335-9610-7 10 TABLET in 1 BOTTLE (71335-9610-7)

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": "0c658a0b-598c-4a44-a00a-7da9cb475f95", "openfda": {"nui": ["N0000175568", "M0003451"], "unii": ["73K4184T59"], "rxcui": ["197604"], "spl_set_id": ["5fb1bc4e-5806-4c50-aab0-91e445d87933"], "pharm_class_cs": ["Cardiac Glycosides [CS]"], "pharm_class_epc": ["Cardiac Glycoside [EPC]"], "manufacturer_name": ["Bryant Ranch Prepack"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET in 1 BOTTLE (71335-9610-1)", "package_ndc": "71335-9610-1", "marketing_start_date": "20240716"}, {"sample": false, "description": "90 TABLET in 1 BOTTLE (71335-9610-2)", "package_ndc": "71335-9610-2", "marketing_start_date": "20221219"}, {"sample": false, "description": "15 TABLET in 1 BOTTLE (71335-9610-3)", "package_ndc": "71335-9610-3", "marketing_start_date": "20240716"}, {"sample": false, "description": "6 TABLET in 1 BOTTLE (71335-9610-4)", "package_ndc": "71335-9610-4", "marketing_start_date": "20230922"}, {"sample": false, "description": "60 TABLET in 1 BOTTLE (71335-9610-5)", "package_ndc": "71335-9610-5", "marketing_start_date": "20240716"}, {"sample": false, "description": "100 TABLET in 1 BOTTLE (71335-9610-6)", "package_ndc": "71335-9610-6", "marketing_start_date": "20240716"}, {"sample": false, "description": "10 TABLET in 1 BOTTLE (71335-9610-7)", "package_ndc": "71335-9610-7", "marketing_start_date": "20240716"}], "brand_name": "Digoxin", "product_id": "71335-9610_0c658a0b-598c-4a44-a00a-7da9cb475f95", "dosage_form": "TABLET", "pharm_class": ["Cardiac Glycoside [EPC]", "Cardiac Glycosides [CS]"], "product_ndc": "71335-9610", "generic_name": "Digoxin", "labeler_name": "Bryant Ranch Prepack", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Digoxin", "active_ingredients": [{"name": "DIGOXIN", "strength": "125 ug/1"}], "application_number": "ANDA076363", "marketing_category": "ANDA", "marketing_start_date": "20150217", "listing_expiration_date": "20261231"}