Warfarin Sodium NDC 50090-5390

NDC codes

FDA NDC Directory

Product NDC (as listed)50090-5390Labeler and product segments. Claims need a package NDC.

Product NDC at billing width50090-5390Add 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
50090-5390-0	50090539000	30 TABLET in 1 BOTTLE (50090-5390-0)Marketed from Nov 23, 2020

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 — 4 mg/1
Dosage form: Tablet
Route: Oral
Labeler: A-S Medication Solutions
Product type: Prescription drug
Marketing category: ANDA — Abbreviated New Drug Application (generic)Application ANDA 040616
Marketing start: Jun 9, 2015
Listing expires: Dec 31, 2027
Other FDA classes: Vitamin K Inhibitors (Mechanism)
Identifiers: Product ID 50090-5390_6a04f416-9063-4129-aa28-655f368db64cSPL ID 6a04f416-9063-4129-aa28-655f368db64c
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

N450090539000 followed by a unit qualifier and the quantity

Package 50090-5390-00. 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

The FDA listing for this product does not reference a label (SPL) set.

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 1 mg/1	TabletOral	Teva Pharmaceuticals USA, Inc.	0093-1712
Warfarin Sodium	Warfarin sodium 5 mg/1	TabletOral	Bryant Ranch Prepack	63629-8843
Warfarin Sodium	Warfarin sodium 2 mg/1	TabletOral	Teva Pharmaceuticals USA, Inc.	0093-1713
Warfarin Sodium	Warfarin sodium 2 mg/1	TabletOral	Northwind Health Company, LLC	51655-993
Warfarin Sodium	Warfarin sodium 2.5 mg/1	TabletOral	Bryant Ranch Prepack	71335-0348
Warfarin Sodium	Warfarin sodium 5 mg/1	TabletOral	Proficient Rx LP	63187-674
Warfarin Sodium	Warfarin sodium 2.5 mg/1	TabletOral	Teva Pharmaceuticals USA, Inc.	0093-1714
Warfarin Sodium	Warfarin sodium 1 mg/1	TabletOral	REMEDYREPACK INC.	70518-0727
Warfarin Sodium	Warfarin sodium 4 mg/1	TabletOral	Teva Pharmaceuticals USA, Inc.	0093-1716
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 6 mg/1	TabletOral	Teva Pharmaceuticals USA, Inc.	0093-1718
Warfarin Sodium	Warfarin sodium 4 mg/1	TabletOral	Bryant Ranch Prepack	71335-0452
Warfarin Sodium	Warfarin sodium 2.5 mg/1	TabletOral	Proficient Rx LP	63187-745
Warfarin Sodium	Warfarin sodium 10 mg/1	TabletOral	Teva Pharmaceuticals USA, Inc.	0093-1720
Warfarin Sodium	Warfarin sodium 7.5 mg/1	TabletOral	Bryant Ranch Prepack	71335-1059
Warfarin Sodium	Warfarin sodium 5 mg/1	TabletOral	PD-Rx Pharmaceuticals, Inc.	43063-176
Warfarin Sodium	Warfarin sodium 10 mg/1	TabletOral	Proficient Rx LP	63187-750
Warfarin Sodium	Warfarin sodium 1 mg/1	TabletOral	Northwind Health Company, LLC	51655-620
Warfarin Sodium	Warfarin sodium 5 mg/1	TabletOral	Teva Pharmaceuticals USA, Inc.	0093-1721

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