NDC codes

FDA NDC Directory
Product NDC (as listed)0143-1240Labeler and product segments. Claims need a package NDC.
Product NDC at billing width00143-1240Add the package segment from the table below.
Package NDCs as listed with the FDA, and the 11-digit 5-4-2 form used on claims. The highlighted digit is the added leading zero.
Package NDC11-digit (billing)PackageCopy
0143-1240-0100143124001100 TABLET in 1 BOTTLE, PLASTIC (0143-1240-01)Marketed from Oct 30, 2007
0143-1240-10001431240101000 TABLET in 1 BOTTLE, PLASTIC (0143-1240-10)Marketed from Oct 30, 2007

How the 11-digit form is made: The labeler segment has 4 digits, so one leading zero is added to it (4-4-2 → 5-4-2). Formatting the NDC does not by itself make it billable — the product, package and quantity must match what was dispensed or administered, and payer rules apply. Conversion rules

Product information

Brand name (proprietary)
Digoxin
Generic name (nonproprietary)
digoxin
Active ingredients
Digoxin — 125 ug/1
Dosage form
Tablet
Route
Oral
Product type
Prescription drug
Marketing category
ANDA — Abbreviated New Drug Application (generic)Application ANDA 077002
Marketing start
Listing expires
Other FDA classes
Cardiac Glycosides (Chemical structure)
Identifiers
Product ID 0143-1240_935f4e33-109c-448c-822c-530145dbbc05SPL ID 935f4e33-109c-448c-822c-530145dbbc05SPL set ID 41c16cff-b03e-405e-a617-d6f45d3ce2bdRxCUI 197604, 197606UNII 73K4184T59UPC 0301431240103, 0301431241100
Pharmacologic class
Cardiac Glycoside

Billing references

What Med-Code can say about coding this product, and where each statement comes from. Nothing here is inferred from the name alone.

HCPCS codeNo match

No HCPCS code in Med-Code's directory. Oral products like this are usually dispensed by a pharmacy and billed by NDC.

NDC on a medical claim

N400143124001 followed by a unit qualifier and the quantity

Package 00143-1240-01. Unit qualifiers: F2 (international unit), GR (gram), ME (milligram), ML (milliliter), UN (unit (each)). The qualifier and quantity depend on what was given. About the N4 qualifier

Product label

Current FDA label (SPL), effective .

Indications (excerpt from the label)

Digoxin Tablets are a cardiac glycoside indicated for: Treatment of mild to moderate heart failure in adults. ( 1.1 ) Increasing myocardial contractility in pediatric patients with heart failure. ( 1.2 ) Control of resting ventricular rate in patients with chronic atrial fibrillation in adults. ( 1.3 ) 1.1 Heart Failure in Adults Digoxin Tablets are indicated for the treatment of mild to moderate heart failure in adults. Digoxin Tablets increase left ventricular ejection fraction and improve heart failure symptoms as evidenced by improved exercise capacity and decreased heart failure-related hospitalizations and emergency care, while having no effect on mortality. Where possible, Digoxin Tab…

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)

Other NDCs under ANDA 077002

Products listed under the same FDA application: other strengths and forms, and repackagers who relabel the same product.

FDA NDC Directory listings under ANDA 077002
ProductStrengthForm · routeLabelerProduct NDC
DigoxinDigoxin 125 ug/1TabletOralNCS HealthCare of KY, LLC dba Vangard Labs0615-8202
DigoxinDigoxin 125 ug/1TabletOralMajor Pharmaceuticals0904-5921
DigoxinDigoxin 250 ug/1TabletOralGolden State Medical Supply, Inc.60429-100
DigoxinDigoxin 250 ug/1TabletOralMajor Pharmaceuticals0904-5922
DigoxinDigoxin 250 ug/1TabletOralHikma Pharmaceuticals USA Inc.0143-1241
DigoxinDigoxin 125 ug/1TabletOralCardinal Health 107, LLC55154-5882

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Digoxin NDC 0143-1240 | Med-Code