What is NDC 67046-1317?

67046-1317 is the product NDC for Digoxin, Digoxin .125 mg/1 tablet, listed with the FDA by Coupler LLC. It has 1 package NDC, shown above in 10- and 11-digit form.

Coupler LLC, NDC labeler code 67046. 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.

Is there a related HCPCS / J-code?

Not in Med-Code's curated HCPCS directory.

Digoxin NDC 67046-1317 | National Drug Code

NDC codes

FDA NDC Directory

Product NDC (as listed)67046-1317Labeler and product segments. Claims need a package NDC.

Product NDC at billing width67046-1317Add 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 NDC	11-digit (billing)	Package	Copy
67046-1317-3	6704613170367046131703	30 TABLET in 1 BLISTER PACK (67046-1317-3)Marketed from Jun 10, 2026

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 — .125 mg/1
Dosage form: Tablet
Route: Oral
Labeler: Coupler LLCNDC labeler code 67046
Product type: Prescription drug
Marketing category: ANDA — Abbreviated New Drug Application (generic)Application ANDA 214982
Marketing start: Jun 10, 2026
Listing expires: Dec 31, 2027
Other FDA classes: Cardiac Glycosides (Chemical structure)
Identifiers: Product ID 67046-1317_53e5a4dc-8479-42f5-e063-6294a90a0c08SPL ID 53e5a4dc-8479-42f5-e063-6294a90a0c08SPL set ID 53e5aec1-052b-454e-e063-6394a90a87f3RxCUI 197604UNII 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

N467046131703 followed by a unit qualifier and the quantity

Package 67046-1317-03. 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 Jun 10, 2026.

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 tablets are indicated for the treatment of mild to moderate heart failure in adults. Digoxin tablets 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 tablets sh…

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)

About NDC 67046-1317

What is NDC 67046-1317?: 67046-1317 is the product NDC for Digoxin, Digoxin .125 mg/1 tablet, listed with the FDA by Coupler LLC. 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?: Coupler LLC, NDC labeler code 67046. 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
Product	Strength	Form · route	Labeler	Product NDC	Package NDCs (11-digit)
Digoxin	Digoxin .25 mg/1	TabletOral	American Health Packaging	60687-869	60687-0869-01
Digoxin	Digoxin .125 mg/1	TabletOral	American Health Packaging	60687-858	60687-0858-01
Digoxin	Digoxin .125 mg/1	TabletOral	AvPAK	50268-238	50268-0238-15
Digoxin	Digoxin .125 mg/1	TabletOral	REMEDYREPACK INC.	70518-3859	70518-3859-00
Digoxin	Digoxin .25 mg/1	TabletOral	REMEDYREPACK INC.	70518-3860	70518-3860-00
Digoxin	Digoxin .125 mg/1	TabletOral	Northwind Health Company, LLC	51655-403	51655-0403-52
Digoxin	Digoxin 125 ug/1	TabletOral	Bryant Ranch Prepack	71335-2463	71335-2463-0171335-2463-02
Digoxin	Digoxin 250 ug/1	TabletOral	Bryant Ranch Prepack	71335-2464	71335-2464-0171335-2464-02
Digoxin	Digoxin 250 ug/1	TabletOral	Bryant Ranch Prepack	71335-3156	71335-3156-0171335-3156-0271335-3156-03+1 more
Digoxin	Digoxin 125 ug/1	TabletOral	Bryant Ranch Prepack	72162-2268	72162-2268-0072162-2268-0172162-2268-02+1 more

All 51 Digoxin NDCs

Other NDCs under ANDA 214982

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

FDA NDC Directory listings under ANDA 214982
Product	Strength	Form · route	Labeler	Product NDC
Digoxin	Digoxin .125 mg/1	TabletOral	A-S Medication Solutions	50090-6708
Digoxin	Digoxin .25 mg/1	TabletOral	A-S Medication Solutions	50090-7865
Digoxin	Digoxin .125 mg/1	TabletOral	AvPAK	50268-238
Digoxin	Digoxin .0625 mg/1	TabletOral	Aurobindo Pharma Limited	59651-436
Digoxin	Digoxin .125 mg/1	TabletOral	Aurobindo Pharma Limited	59651-437
Digoxin	Digoxin .25 mg/1	TabletOral	Aurobindo Pharma Limited	59651-438
Digoxin	Digoxin .125 mg/1	TabletOral	REMEDYREPACK INC.	70518-3859
Digoxin	Digoxin .25 mg/1	TabletOral	REMEDYREPACK INC.	70518-3860