NDC codes

FDA NDC Directory
Product NDC (as listed)68180-709Labeler and product segments. Claims need a package NDC.
Product NDC at billing width68180-0709Add 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
68180-709-066818007090630 TABLET, FILM COATED in 1 BOTTLE (68180-709-06)Marketed from Mar 6, 2025
68180-709-096818007090990 TABLET, FILM COATED in 1 BOTTLE (68180-709-09)Marketed from Mar 6, 2025

How the 11-digit form is made: The product segment has 3 digits, so one leading zero is added to it (5-3-2 → 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)
Rivaroxaban
Generic name (nonproprietary)
rivaroxaban
Active ingredients
Rivaroxaban — 2.5 mg/1
Dosage form
Tablet, Film coated
Route
Oral
Product type
Prescription drug
Marketing category
ANDA — Abbreviated New Drug Application (generic)Application ANDA 208555
Marketing start
Listing expires
Other FDA classes
Factor Xa Inhibitors (Mechanism)
Identifiers
Product ID 68180-709_310f0bf6-9b0f-441b-afd7-b9a0f7905395SPL ID 310f0bf6-9b0f-441b-afd7-b9a0f7905395SPL set ID 702fed3e-ae25-49ba-98cc-562e0e244214RxCUI 2059015UNII 9NDF7JZ4M3UPC 0368180709060
Pharmacologic class
Factor Xa Inhibitor

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

N468180070906 followed by a unit qualifier and the quantity

Package 68180-0709-06. 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 . This label includes a boxed warning.

Indications (excerpt from the label)

Rivaroxaban is a factor Xa inhibitor indicated: to reduce the risk of major cardiovascular events in patients with coronary artery disease (CAD) ( 1.7 ) to reduce the risk of major thrombotic vascular events in patients with peripheral artery disease (PAD), including patients after recent lower extremity revascularization due to symptomatic PAD ( 1.8 ) 1.7 Reduction of Risk of Major Cardiovascular Events in Patients with Coronary Artery Disease (CAD) Rivaroxaban tablets, in combination with aspirin, are indicated to reduce the risk of major cardiovascular events (cardiovascular death, myocardial infarction, and stroke) in adult patients with coronary artery disease. 1.8 Reduction of Risk of …

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)

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