NDC codes

FDA NDC Directory
Product NDC (as listed)50090-5862Labeler and product segments. Claims need a package NDC.
Product NDC at billing width50090-5862Add 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
50090-5862-15009058620150090586201100 TABLET in 1 BOTTLE (50090-5862-1)Marketed from Nov 26, 2021

How the 11-digit form is made: The package segment has 1 digit, so one leading zero is added to it (5-4-1 → 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 — 250 ug/1
Dosage form
Tablet
Route
Oral
Labeler
A-S Medication SolutionsNDC labeler code 50090
Product type
Prescription drug
Marketing category
ANDA — Abbreviated New Drug Application (generic)Application ANDA 076363
Marketing start
Listing expires
Other FDA classes
Cardiac Glycosides (Chemical structure)
Identifiers
Product ID 50090-5862_c7f8d15e-5ae7-431d-ae43-1ad93910b3ecSPL ID c7f8d15e-5ae7-431d-ae43-1ad93910b3ecSPL set ID aea39b37-951e-49e8-9756-c763c0e7c7cdRxCUI 197606UNII 73K4184T59
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

N450090586201 followed by a unit qualifier and the quantity

Package 50090-5862-01. 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 is 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 is indicated for the treatment of mild to moderate heart failure in adults. Digoxin increases left ventricular ejection fraction and improves 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 should be used in combin…

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)

About NDC 50090-5862

What is NDC 50090-5862?
50090-5862 is the product NDC for Digoxin, Digoxin 250 ug/1 tablet, listed with the FDA by A-S Medication Solutions. It has 1 package NDC, shown above in 10- and 11-digit form.
What drug is associated with this NDC?
Digoxin.
What is the active ingredient?
Digoxin.
Who is the labeler?
A-S Medication Solutions, NDC labeler code 50090. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.
What other NDCs exist for Digoxin?
50 other product NDCs are listed under this name. See all Digoxin NDCs.
Is there a related HCPCS / J-code?
Not in Med-Code's curated HCPCS directory. See Billing references above.

Other finished products listed under the same name: strengths, forms and labelers.

Other Digoxin NDCs
ProductStrengthForm · routeLabelerProduct NDCPackage NDCs (11-digit)
DigoxinDigoxin .125 mg/1TabletOralCoupler LLC67046-131767046-1317-03
DigoxinDigoxin .25 mg/1TabletOralAmerican Health Packaging60687-86960687-0869-01
DigoxinDigoxin .125 mg/1TabletOralAmerican Health Packaging60687-85860687-0858-01
DigoxinDigoxin .125 mg/1TabletOralAvPAK50268-23850268-0238-15
DigoxinDigoxin .125 mg/1TabletOralREMEDYREPACK INC.70518-385970518-3859-00
DigoxinDigoxin .25 mg/1TabletOralREMEDYREPACK INC.70518-386070518-3860-00
DigoxinDigoxin .125 mg/1TabletOralNorthwind Health Company, LLC51655-40351655-0403-52
DigoxinDigoxin 125 ug/1TabletOralBryant Ranch Prepack71335-246371335-2463-0171335-2463-02
DigoxinDigoxin 250 ug/1TabletOralBryant Ranch Prepack71335-246471335-2464-0171335-2464-02
DigoxinDigoxin 250 ug/1TabletOralBryant Ranch Prepack71335-315671335-3156-0171335-3156-0271335-3156-03+1 more

All 51 Digoxin NDCs

Other NDCs under ANDA 076363

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

FDA NDC Directory listings under ANDA 076363
ProductStrengthForm · routeLabelerProduct NDC
DigoxinDigoxin 125 ug/1TabletOralA-S Medication Solutions50090-5642
DigoxinDigoxin 250 ug/1TabletOralA-S Medication Solutions50090-6588

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