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Brand-name prescription medicine

Rivaroxaban Granule

Generic name: Rivaroxaban

FDA application holder: Lupin

Official data, not advice

Everything here comes from the U.S. Food and Drug Administration (FDA): the NDC Directory, Drugs@FDA, the official labels and recall reports; pharmacy costs come from the Centers for Medicare & Medicaid Services (CMS). Each fact shows its source and date.

This page is not medical advice. Talk to your doctor or pharmacist before you start, stop or switch any medicine, including a switch between a brand and a generic.

In an emergency, call 911. If someone may have taken too much of a medicine, call Poison Help: 1‑800‑222‑1222.

Quick answers

What is Rivaroxaban Granule?
Rivaroxaban Granule is a brand name of Rivaroxaban, a prescription medicine. The FDA NDC Directory lists 1 Rivaroxaban Granule product in 1 strength and form.
Who makes Rivaroxaban Granule?
Lupin holds the FDA application for Rivaroxaban Granule (ANDA218195, approved September 25, 2025).
Is there a generic or store brand of Rivaroxaban Granule?
Other products of Rivaroxaban are listed with the FDA, but none in exactly the same strength and form as a Rivaroxaban Granule product.
What do pharmacies pay for Rivaroxaban Granule?
CMS lists a National Average Drug Acquisition Cost (NADAC) for 1 Rivaroxaban Granule strength and form (see the table below). That is what pharmacies pay to buy it, not what you pay: your price depends on your insurance and your pharmacy.
Has Rivaroxaban Granule been recalled?
No recall linked to Rivaroxaban Granule products (by their NDC code or label) appears in the FDA enforcement reports we use.

What Rivaroxaban Granule is

Each Rivaroxaban Granule product as listed in the FDA NDC Directory, by active ingredient, strength and form, with its official label. “Same medicine, other names” counts the other products with exactly the same active ingredients, strength and form (generic versions, store brands and other brands); inactive ingredients can differ.

Rivaroxaban · prescription medicine

Strength and formProduct namesSame medicine, other namesLabel
rivaroxaban 155 mg
for suspension (oral)
Rivaroxaban Granule None listed DailyMed

Its page lists every product and company, the FDA label’s uses and boxed warning, approvals, shortages and recalls: Rivaroxaban →

FDA approval

  • ANDA: Abbreviated New Drug Application: how a generic version is approved.
FDA applications of Rivaroxaban Granule products (Drugs@FDA)
ApplicationHolderFirst approvedProducts
ANDA218195LupinSeptember 25, 20251

What pharmacies pay (NADAC)

The National Average Drug Acquisition Cost (NADAC) is the average price U.S. retail pharmacies paid to buy one unit of a medicine (one tablet, one mL or one gram), from a monthly survey of pharmacy invoices by the Centers for Medicare & Medicaid Services (CMS). State Medicaid programs use it to pay pharmacies.

This is not the price you pay. What you pay depends on your insurance (copay or coinsurance), your pharmacy and any discounts, and pharmacies also charge for filling a prescription. Ask your pharmacist or your health plan what your price will be.

NADAC per unit for Rivaroxaban Granule, by strength and form
Strength and formGeneric or brandPharmacies pay
rivaroxaban 155 mg
for suspension
Generic: Rivaroxaban Granule $1.81 per mL
Generic of the same strength and form: $1.81 per mL

NADAC list of November 4, 2026; these prices took effect on October 21, 2026. Shown only where a package’s NDC code matches the NADAC list exactly, and only for that exact strength and form: nothing is averaged across strengths. Strengths and forms not listed here have no NADAC price.

Source: NADAC (National Average Drug Acquisition Cost) 2026, data.medicaid.gov (CMS) →

Companies that list Rivaroxaban Granule

The company named on the package (holder, repackager or distributor), as listed in the FDA NDC Directory, with its number of Rivaroxaban Granule products.

Recalls

No recall linked to Rivaroxaban Granule products (by their NDC code or label) appears in the FDA enforcement reports.

Sources

  1. NDC Directory (openFDA) — U.S. Food and Drug Administration (FDA), FDA data exported October 30, 2026, retrieved October 31, 2026
  2. Drugs@FDA (openFDA) — U.S. Food and Drug Administration (FDA), FDA data exported October 30, 2026, retrieved October 31, 2026
  3. Drug labeling (SPL, openFDA) — U.S. Food and Drug Administration (FDA), FDA data exported October 30, 2026, retrieved October 31, 2026
  4. Drug recall enforcement reports (openFDA) — U.S. Food and Drug Administration (FDA), FDA data exported October 27, 2026, retrieved October 31, 2026
  5. NADAC (National Average Drug Acquisition Cost) 2026 — Centers for Medicare & Medicaid Services (CMS), data.medicaid.gov, list of November 4, 2026, retrieved November 7, 2026

Which names get a brand page: a name the NDC Directory lists for a medicine, held by one company (the FDA application holder, or the company named on most of its products), that is not just a description, and that is not the only product of its medicine.

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