What is NDC 71335-0243?

71335-0243 is the product NDC for Warfarin Sodium, Warfarin sodium 5 mg/1 tablet, listed with the FDA by Bryant Ranch Prepack. It has 6 package NDCs, shown above in 10- and 11-digit form.

Bryant Ranch Prepack, NDC labeler code 71335. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.

What other NDCs exist for Warfarin Sodium?

138 other product NDCs are listed under this name.

Is there a related HCPCS / J-code?

Not in Med-Code's curated HCPCS directory.

Warfarin Sodium NDC 71335-0243 | National Drug Code

NDC codes

FDA NDC Directory

Product NDC (as listed)71335-0243Labeler and product segments. Claims need a package NDC.

Product NDC at billing width71335-0243Add 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
71335-0243-1	7133502430171335024301	100 TABLET in 1 BOTTLE (71335-0243-1)Marketed from Apr 26, 2018
71335-0243-2	7133502430271335024302	30 TABLET in 1 BOTTLE (71335-0243-2)Marketed from Jul 13, 2018
71335-0243-3	7133502430371335024303	45 TABLET in 1 BOTTLE (71335-0243-3)Marketed from Dec 27, 2021
71335-0243-4	7133502430471335024304	60 TABLET in 1 BOTTLE (71335-0243-4)Marketed from Apr 9, 2018
71335-0243-5	7133502430571335024305	15 TABLET in 1 BOTTLE (71335-0243-5)Marketed from Dec 27, 2021
71335-0243-6	7133502430671335024306	90 TABLET in 1 BOTTLE (71335-0243-6)Marketed from Jun 22, 2018

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): Warfarin Sodium
Generic name (nonproprietary): warfarin sodium
Active ingredients: Warfarin sodium — 5 mg/1
Dosage form: Tablet
Route: Oral
Labeler: Bryant Ranch PrepackNDC labeler code 71335
Product type: Prescription drug
Marketing category: ANDA — Abbreviated New Drug Application (generic)Application ANDA 040616
Marketing start: Apr 7, 2015
Listing expires: Dec 31, 2026
Other FDA classes: Vitamin K Inhibitors (Mechanism)
Identifiers: Product ID 71335-0243_578c0776-7e59-4edb-9929-0975fb01a8d4SPL ID 578c0776-7e59-4edb-9929-0975fb01a8d4SPL set ID 44077bb7-6007-4c15-bbcd-a7a02ac081ceRxCUI 855332UNII 6153CWM0CL
Pharmacologic class: Vitamin K Antagonist

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

N471335024301 followed by a unit qualifier and the quantity

Package 71335-0243-01. 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 Jul 14, 2025. This label includes a boxed warning.

Indications (excerpt from the label)

Warfarin sodium tablets are indicated for: Prophylaxis and treatment of venous thrombosis and its extension, pulmonary embolism (PE). Prophylaxis and treatment of thromboembolic complications associated with atrial fibrillation (AF) and/or cardiac valve replacement. Reduction in the risk of death, recurrent myocardial infarction (MI), and thromboembolic events such as stroke or systemic embolization after myocardial infarction. Limitations of Use Warfarin sodium tablets have no direct effect on an established thrombus, nor does it reverse ischemic tissue damage. Once a thrombus has occurred, however, the goals of anticoagulant treatment are to prevent further extension of the formed clot and…

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)

About NDC 71335-0243

What is NDC 71335-0243?: 71335-0243 is the product NDC for Warfarin Sodium, Warfarin sodium 5 mg/1 tablet, listed with the FDA by Bryant Ranch Prepack. It has 6 package NDCs, shown above in 10- and 11-digit form.
What drug is associated with this NDC?: Warfarin Sodium.
What is the active ingredient?: Warfarin sodium.
Who is the labeler?: Bryant Ranch Prepack, NDC labeler code 71335. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.
What other NDCs exist for Warfarin Sodium?: 138 other product NDCs are listed under this name. See all Warfarin Sodium 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 Warfarin Sodium NDCs
Product	Strength	Form · route	Labeler	Product NDC	Package NDCs (11-digit)
Warfarin Sodiumwarfarin	Warfarin sodium 2.5 mg/1	TabletOral	Coupler LLC	67046-1145	67046-1145-03
Warfarin Sodiumwarfarin	Warfarin sodium 3 mg/1	TabletOral	Coupler LLC	67046-1185	67046-1185-03
Warfarin Sodium	Warfarin sodium 3 mg/1	TabletOral	REMEDYREPACK INC.	70518-4722	70518-4722-00
Warfarin Sodiumwarfarin	Warfarin sodium 10 mg/1	TabletOral	REMEDYREPACK INC.	70518-4684	70518-4684-00
Warfarin Sodiumwarfarin	Warfarin sodium 1 mg/1	TabletOral	Coupler LLC	67046-2072	67046-2072-03
Warfarin Sodiumwarfarin	Warfarin sodium 2 mg/1	TabletOral	Coupler LLC	67046-1067	67046-1067-03
Warfarin Sodium	Warfarin sodium 2.5 mg/1	TabletOral	REMEDYREPACK INC.	70518-4634	70518-4634-00
Warfarin Sodium	Warfarin sodium 7.5 mg/1	TabletOral	REMEDYREPACK INC.	70518-4635	70518-4635-00
Warfarin Sodium	Warfarin sodium 10 mg/1	TabletOral	REMEDYREPACK INC.	70518-4636	70518-4636-00
Warfarin Sodium	Warfarin sodium 1 mg/1	TabletOral	REMEDYREPACK INC.	70518-4637	70518-4637-00

All 139 Warfarin Sodium NDCs

Other NDCs under ANDA 040616

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

FDA NDC Directory listings under ANDA 040616
Product	Strength	Form · route	Labeler	Product NDC
Warfarin Sodium	Warfarin sodium 2 mg/1	TabletOral	REMEDYREPACK INC.	70518-0255
Warfarin Sodium	Warfarin sodium 6 mg/1	TabletOral	REMEDYREPACK INC.	70518-0261
Warfarin Sodium	Warfarin sodium 4 mg/1	TabletOral	REMEDYREPACK INC.	70518-0280
Warfarin Sodium	Warfarin sodium 10 mg/1	TabletOral	REMEDYREPACK INC.	70518-0266
Warfarin Sodium	Warfarin sodium 3 mg/1	TabletOral	REMEDYREPACK INC.	70518-0273
Warfarin Sodium	Warfarin sodium 5 mg/1	TabletOral	A-S Medication Solutions	50090-5439
Warfarin Sodium	Warfarin sodium 5 mg/1	TabletOral	A-S Medication Solutions	50090-5440
Warfarin Sodium	Warfarin sodium 5 mg/1	TabletOral	Bryant Ranch Prepack	63629-8843
Warfarin Sodium	Warfarin sodium 2 mg/1	TabletOral	Northwind Health Company, LLC	51655-993
Warfarin Sodium	Warfarin sodium 10 mg/1	TabletOral	Bryant Ranch Prepack	71335-0840
Warfarin Sodium	Warfarin sodium 5 mg/1	TabletOral	Proficient Rx LP	63187-674
Warfarin Sodium	Warfarin sodium 1 mg/1	TabletOral	REMEDYREPACK INC.	70518-0727
Warfarin Sodium	Warfarin sodium 1 mg/1	TabletOral	Bryant Ranch Prepack	71335-0270
Warfarin Sodium	Warfarin sodium 2 mg/1	TabletOral	A-S Medication Solutions	50090-7464
Warfarin Sodium	Warfarin sodium 2.5 mg/1	TabletOral	Proficient Rx LP	63187-745
Warfarin Sodium	Warfarin sodium 10 mg/1	TabletOral	Proficient Rx LP	63187-750
Warfarin Sodium	Warfarin sodium 2.5 mg/1	TabletOral	Bryant Ranch Prepack	71335-0348
Warfarin Sodium	Warfarin sodium 1 mg/1	TabletOral	Northwind Health Company, LLC	51655-620
Warfarin Sodium	Warfarin sodium 5 mg/1	TabletOral	Northwind Health Company, LLC	51655-629
Warfarin Sodium	Warfarin sodium 10 mg/1	TabletOral	A-S Medication Solutions	50090-7229

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