Prescription drug · ANDA

Warfarin Sodium (Warfarin) NDC 50090-2582

Warfarin sodium 7.5 mg/1 · Tablet · Oral · A-S Medication Solutions

NDC codes

FDA NDC Directory
Product NDC (as listed)50090-2582Labeler and product segments. Claims need a package NDC.
Product NDC at billing width50090-2582Add 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
50090-2582-0500902582005009025820030 TABLET in 1 BOTTLE (50090-2582-0)Marketed from Nov 1, 2016

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
Active ingredients
Warfarin sodium — 7.5 mg/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 202202
Marketing start
Listing expires
Other FDA classes
Vitamin K Inhibitors (Mechanism)
Identifiers
Product ID 50090-2582_af41a188-068e-42ec-bb07-e921815b791eSPL ID af41a188-068e-42ec-bb07-e921815b791e
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

N450090258200 followed by a unit qualifier and the quantity

Package 50090-2582-00. 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.

About NDC 50090-2582

What is NDC 50090-2582?
50090-2582 is the product NDC for Warfarin Sodium (warfarin), Warfarin sodium 7.5 mg/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?
Warfarin Sodium (Warfarin).
What is the active ingredient?
Warfarin sodium.
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 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
ProductStrengthForm · routeLabelerProduct NDCPackage NDCs (11-digit)
Warfarin SodiumwarfarinWarfarin sodium 2.5 mg/1TabletOralCoupler LLC67046-114567046-1145-03
Warfarin SodiumwarfarinWarfarin sodium 3 mg/1TabletOralCoupler LLC67046-118567046-1185-03
Warfarin SodiumWarfarin sodium 3 mg/1TabletOralREMEDYREPACK INC.70518-472270518-4722-00
Warfarin SodiumwarfarinWarfarin sodium 10 mg/1TabletOralREMEDYREPACK INC.70518-468470518-4684-00
Warfarin SodiumwarfarinWarfarin sodium 1 mg/1TabletOralCoupler LLC67046-207267046-2072-03
Warfarin SodiumwarfarinWarfarin sodium 2 mg/1TabletOralCoupler LLC67046-106767046-1067-03
Warfarin SodiumWarfarin sodium 2.5 mg/1TabletOralREMEDYREPACK INC.70518-463470518-4634-00
Warfarin SodiumWarfarin sodium 7.5 mg/1TabletOralREMEDYREPACK INC.70518-463570518-4635-00
Warfarin SodiumWarfarin sodium 10 mg/1TabletOralREMEDYREPACK INC.70518-463670518-4636-00
Warfarin SodiumWarfarin sodium 1 mg/1TabletOralREMEDYREPACK INC.70518-463770518-4637-00

All 139 Warfarin Sodium NDCs

Other NDCs under ANDA 202202

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

FDA NDC Directory listings under ANDA 202202
ProductStrengthForm · routeLabelerProduct NDC
Warfarin SodiumwarfarinWarfarin sodium 2.5 mg/1TabletOralA-S Medication Solutions50090-2586
Warfarin SodiumwarfarinWarfarin sodium 3 mg/1TabletOralA-S Medication Solutions50090-2613
Warfarin SodiumwarfarinWarfarin sodium 6 mg/1TabletOralA-S Medication Solutions50090-2617
Warfarin SodiumwarfarinWarfarin sodium 4 mg/1TabletOralA-S Medication Solutions50090-2645
Warfarin SodiumwarfarinWarfarin sodium 1 mg/1TabletOralA-S Medication Solutions50090-2646
Warfarin SodiumwarfarinWarfarin sodium 5 mg/1TabletOralA-S Medication Solutions50090-2936
Warfarin SodiumwarfarinWarfarin sodium 1 mg/1TabletOralAmneal Pharmaceuticals LLC65162-761
Warfarin SodiumwarfarinWarfarin sodium 2 mg/1TabletOralAmneal Pharmaceuticals LLC65162-762
Warfarin SodiumwarfarinWarfarin sodium 2.5 mg/1TabletOralAmneal Pharmaceuticals LLC65162-763
Warfarin SodiumwarfarinWarfarin sodium 3 mg/1TabletOralAmneal Pharmaceuticals LLC65162-764
Warfarin SodiumwarfarinWarfarin sodium 4 mg/1TabletOralAmneal Pharmaceuticals LLC65162-765
Warfarin SodiumwarfarinWarfarin sodium 5 mg/1TabletOralAmneal Pharmaceuticals LLC65162-766
Warfarin SodiumwarfarinWarfarin sodium 6 mg/1TabletOralAmneal Pharmaceuticals LLC65162-767
Warfarin SodiumwarfarinWarfarin sodium 7.5 mg/1TabletOralAmneal Pharmaceuticals LLC65162-768
Warfarin SodiumwarfarinWarfarin sodium 10 mg/1TabletOralAmneal Pharmaceuticals LLC65162-769
Warfarin SodiumwarfarinWarfarin sodium 2 mg/1TabletOralCoupler LLC67046-1067
Warfarin SodiumwarfarinWarfarin sodium 2.5 mg/1TabletOralCoupler LLC67046-1145
Warfarin SodiumwarfarinWarfarin sodium 3 mg/1TabletOralCoupler LLC67046-1185
Warfarin SodiumwarfarinWarfarin sodium 4 mg/1TabletOralCoupler LLC67046-1463
Warfarin SodiumwarfarinWarfarin sodium 7.5 mg/1TabletOralCoupler LLC67046-1525

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