Nabumetone 750 mg Tablet, 100-count
by ASCLEMED USA INC. · 100 TABLET in 1 BOTTLE (87063-292-01)
NDC 87063-0292-01
🏷️ FDA NDC (as labeled)
87063-292-01
billing pads the product segment with a zero
This package
Contains100-count
Pack sizes8 compare ↓
Also comes in:
6 tablets 87063-0292-06
7 tablets 87063-0292-07
10 tablets 87063-0292-10
20 tablets 87063-0292-20
30 tablets 87063-0292-30
60 tablets 87063-0292-60
90 tablets 87063-0292-90
Rx only
Generic
On market
Non-controlled
🗂️ Data synced Aug 27, 2026 · sources: openFDA · FDA label (DailyMed) · FDA Orange & Purple Book · First Databank · CMS NADAC, ASP, Medicare & Medicaid · RxNorm
📋 All sources & update times →
🆔 Identity & classification
FDA NDC (as labeled)
87063-292-01
Product NDC
87063-292
11-digit billing NDC
87063029201
Application #
ANDA078420
SPL Set ID
595fd0eb-93f8-a085-e063-6294a90a46ea
Established class (EPC)
Anti-Inflammatory Agents; Nonsteroidal Anti-inflammatory Drug
Mechanism of action
Cyclooxygenase Inhibitors
Chemical class
Non-Steroidal
DEA schedule
Non-controlled
Marketing category
ANDA
Marketing status
On market
FDA listing status
Listed (active directory)
Marketing start
2019-06-26
Route
ORAL
Dosage form
TABLET
Substance
NABUMETONE
TE code (Orange Book)
AB · RLD · RS
Why two NDCs?
The FDA registers this code as 87063-292-01 — a 5-3-2 layout, and that's what's printed on the package and shown on DailyMed. For insurance claims, every NDC is standardized to a uniform 11-digit 5-4-2 format by adding a zero to the product segment → 87063-0292-01. Same drug, same package — only the format differs.
Where does this data come from?
Identifiers from the FDA openFDA NDC Directory and Structured Product Labeling; RxCUI from RxNorm (NLM); GPI from Medi-Span; GCN / HIC / AHFS / legend from First Databank.
🏭 Manufacturer & labeler
LabelerASCLEMED USA INC.
Application holderSCIEGEN PHARMACEUTICALS INC
FDA applicationANDA078420 (ANDA)
Labeler code87063
First marketedJun 2019
Product typeHuman Prescription Drug
Portfolio122 products on file
The labeler markets the product; the application holder owns the FDA approval. They’re often the same company but can differ (e.g. a repackager or an authorized generic). A mailing address / phone appears here when the manufacturer includes it in the product’s FDA label (not all do).
Where does this data come from?
Labeler, application holder and registered establishment from the FDA openFDA NDC Directory and Drugs@FDA; address/contact from the product’s FDA label.
🩺 Clinical
📗 Our plain-language guide HelloPharmacist
- Nabumetone is a prescription anti-inflammatory medication used to ease the pain, swelling, and stiffness that come with osteoarthritis and rheumatoid arthritis. It won't cure arthr...
- Yes, you can take it with or without food — both are fine. Taking it with food or milk does speed up how quickly it gets into your system, so if you want faster relief, with a meal...
- Can I take nabumetone with food? Does it matter?
- The most common ones are digestive — things like diarrhea, indigestion, and stomach pain. Those are bothersome but usually manageable. What you really want to watch out for are bla...
Patient education
Supplement & herbal interactions
Some supplements/herbs that may interact with Nabumetone — tap one for details:
1
Nutrient depletion considerations
Nabumetone may be associated with lower levels of 1 nutrient — worth a chat with your pharmacist, not a cause for alarm.
An association is not a deficiency. Educational only — don't start or stop anything without professional guidance.
Where does this data come from?
Plain-language summary from MedlinePlus (U.S. National Library of Medicine); supplement & herbal interactions and nutrient depletion data from the Natural Medicines database; our full guide is HelloPharmacist editorial content.
💬 Questions about Nabumetone?
Ask a pharmacist →
Ask a licensed pharmacist directly — free, answered by our team.
🧪 Inactive Ingredients / Excipients
Inactive ingredients, also called excipients, are components of the drug product other than the active ingredient. They may include fillers, dyes, coatings, preservatives, flavors, or other formulation ingredients.
We could not link this NDC to a current FDA Structured Product Label. An inactive-ingredient list is therefore not available from this source.
Where does this data come from?
Source: official FDA Structured Product Labeling (SPL) via DailyMed and the openFDA label index. Structured
IACT rows and label-wide narrative are kept separate; availability and product-level specificity depend on the submitted label.Inactive ingredient FAQ
Are inactive ingredients the same for every manufacturer?
No. Inactive ingredients can differ by manufacturer, dosage form, strength, and package / product version.
Why might an inactive ingredient be missing?
Some SPLs do not provide a complete structured inactive-ingredient list, and older or unusual labels may only include the information in narrative text.
Can inactive ingredients matter?
Yes. They can matter for allergies, intolerances, dyes, gluten / lactose concerns, preservatives, and formulation differences — but confirm with a pharmacist or the manufacturer when it’s clinically important.
💲 Pricing
A drug doesn't have one price. Each row is a different public payment system, and none is what you'd pay at the counter — that depends on your insurance. The ⓘ on each row explains what it measures.
| Price system | Per each | Per package |
|---|---|---|
| Retail pharmacies payNADAC · weekly | Not in the retail survey — common for institutional, discontinued, or low-volume packs. | |
| Medicaid paysCMS SDUD · 12 mo | No recent Medicaid claims on file for this NDC — rare and low-volume NDCs are suppressed in the public data. | |
| Medicare drug plans payPart D · quarterly | No Part D plan price is available for this NDC in our data. | |
ℹ️
No price is published for this exact package yet. CMS surveys NADAC per package size, so a different pack of the same drug often has one.
Where does this data come from?
NADAC (National Average Drug Acquisition Cost) is the CMS weekly pharmacy-acquisition-cost survey — what pharmacies pay. ASP (Average Sales Price) is the CMS Medicare Part B drug-payment file, published quarterly. Medicaid pays is computed by us from CMS State Drug Utilization Data (total reimbursed ÷ units, trailing 12 months) — gross of rebates and inclusive of dispensing fees, so it reflects what Medicaid paid, not an acquisition cost. Medicare drug plans pay is the median negotiated point-of-sale unit cost across plans listing this NDC in the CMS quarterly Prescription Drug Plan pricing files, before rebates. The VA pays is the federal contract price (FSS, and the statutory Big 4 ceiling where listed) from the VA National Acquisition Center pharmaceutical price file. All are free public government data; each measures a different payer, so the figures are not directly comparable.
🔁 Therapeutic equivalents
| Product | Labeler | Pack | NADAC/unit | TE | Status | Price vs. this |
|---|---|---|---|---|---|---|
| Nabumetone 750 mg 62135-0146-60 | Chartwell | 60 tablets | $0.181 | AB | Availability likely | — |
| Nabumetone 750 mg 00591-3671-01 | Actavis | 100 tablets | $0.181 | AB | Availability likely | — |
| Nabumetone 750 mg 50228-0466-01 | ScieGen | 100 tablets | $0.181 | AB | Availability likely | — |
| Nabumetone 750 mg 69097-0966-07 | Cipla | 100 tablets | $0.181 | AB | Availability likely | — |
| Nabumetone 750 mg 70954-0785-10 | ANI | 100 tablets | $0.181 | AB | Availability likely | — |
| Nabumetone 750 mg 76282-0258-01 | Exelan | 100 tablets | $0.181 | AB | Availability likely | — |
| Nabumetone 750 mg 69367-0242-01 | Westminster | 100 tablets | $0.181 | AB | Availability likely | — |
| Nabumetone 750 mg 63187-0307-30 | Proficient | 30 tablets | — | AB | FDA listed | — |
| Nabumetone 750 mg 71205-0530-30 | Proficient | 30 tablets | — | AB | FDA listed | — |
| Nabumetone 750 mg 71205-0978-00 | Proficient | 100 tablets | — | AB | FDA listed | — |
| Nabumetone 750 mg 72789-0540-14 | PD-Rx | 14 tablets | — | AB | FDA listed | — |
| Nabumetone 750 mg 80425-0104-01 | Advanced | 30 tablets | — | AB | FDA listed | — |
| Nabumetone 750 mg 55700-0840-30 | Quality | 30 tablets | — | AB | Discontinued | — |
| Nabumetone 750 mg 60760-0369-14 | St. | 14 tablets | — | AB | FDA listed | — |
| Nabumetone 750 mg 63629-8509-01 | Bryant | 500 tablets | — | AB | FDA listed | — |
| Nabumetone 750 mg 63629-8510-01 | Bryant | 100 tablets | — | AB | FDA listed | — |
| Nabumetone 750 mg 70518-4047-00 | REMEDYREPACK | 14 tablets | — | AB | FDA listed | — |
| Nabumetone 750 mg 72162-1558-01 | Bryant | 100 tablets | — | AB | FDA listed | — |
| Nabumetone 750 mg 51655-0733-52 | Northwind | 30 tablets | — | AB | FDA listed | — |
| Nabumetone 750 mg 71335-1272-00 | Bryant | 7 tablets | — | AB | Discontinued | — |
| Nabumetone 750 mg 72789-0040-30 | PD-Rx | 30 tablets | — | AB | FDA listed | — |
| Nabumetone 750 mg 79739-7077-01 | LGM | 100 tablets | — | — | FDA listed | — |
| Nabumetone 750 mg 68788-7597-01 | Preferred | 100 tablets | — | AB | FDA listed | — |
| Nabumetone 750 mg 72189-0072-14 | direct | 14 tablets | — | AB | FDA listed | — |
| Nabumetone 750 mg 71335-1559-00 | Bryant | 7 tablets | — | AB | Discontinued | — |
| Nabumetone 750 mg 71335-2293-01 | Bryant | 500 tablets | — | AB | FDA listed | — |
| Nabumetone 750 mg 50090-6167-00 | A-S | 30 tablets | — | AB | FDA listed | — |
| Nabumetone 750 mgthis 87063-0292-01 | ASCLEMED | 100 tablets | — | AB | FDA listed | — |
| Nabumetone 750 mg 85766-0262-01 | Sportpharm | 100 tablets | — | AB | FDA listed | — |
About this product: this is a generic version of the medicine. FDA equivalence ratings are shown when available, and other versions are listed above, least expensive first.
Where does this data come from?
Equivalents are other NDCs of the same ingredient, form and route from the openFDA NDC Directory, ranked least-expensive-first by NADAC. Therapeutic-equivalence (AB) ratings come from the FDA Orange Book; biologics use the FDA Purple Book for biosimilar & interchangeable status.
⏳ Availability & generic status
🏛️
2019
On the market since
Jun 2019
📍
2026
Currently FDA-listed
7 years listed
🔓
·
Generic on the market
this product is a generic
✅This is a generic drug
This product is an FDA-approved generic. Other versions of the same drug are listed under Therapeutic equivalents, least expensive first.
Where does this data come from?
Patents and exclusivity from the FDA Orange Book (small-molecule drugs), refreshed from public FDA data. Generic launch timing is an estimate, not a guarantee.
📊 Medicare Part D spend CMS · PART D · 2026 (Q1)
Medicare Part D (outpatient prescription) spending for Nabumetone — the program that covers self-administered drugs. 6 manufacturers.
⚠️ Drug-level data: CMS publishes Part D spending by drug, not by NDC — these figures combine every manufacturer, strength and package size sold under the name Nabumetone. That’s a different level of aggregation than the Medicaid card above, which is specific to this exact 11-digit NDC (pack size included), so the two aren’t directly comparable.
Period
Total Part D spend
$2.22M
Claims incl. refills
130.3K
Beneficiaries
89.2K
Spend / beneficiary
$24.84
Spend / claim
$17.01
Trend by period
💵 About the dollar figures: spending is what Part D plans paid before confidential manufacturer rebates, so the program’s real net cost is lower. A blank patient count means fewer than 11 people — CMS hides counts that small to protect privacy. Source: CMS Medicare Quarterly Part D Spending by Drug (data.cms.gov), updated quarterly.
🔬 Reported adverse events (FAERS)
Read carefully: FAERS reports are voluntary and unverified. Counts are not incidence, do not establish causation, are subject to reporting bias, and cannot be used to compare one drug to another. Shown for signal context only. Reports for Nabumetone — the ingredient across all brands.
Top reported reactions
Age at onset
Reporter sex
Male · 26%
Female · 74%
Unknown · 0%
Serious outcomes
Reports over time (by year) — tap or hover for the count & year
Most recent year is provisional (FAERS lags ~3 months).
Where does this data come from?
Adverse-event reports from the FDA Adverse Event Reporting System (FAERS) via openFDA. FAERS reports are voluntary and unverified — counts are not incidence and don’t establish causation.
📦 Packaging — all sizes for this product
| Package NDC | Description | Marketing start | Status |
|---|---|---|---|
| 87063-0292-01 You're viewing this | 100 TABLET in 1 BOTTLE (87063-292-01) | 2026-08-19 | Active |
| 87063-0292-06 | 6 TABLET in 1 BOTTLE (87063-292-06) | 2026-08-19 | Active |
| 87063-0292-07 | 7 TABLET in 1 BOTTLE (87063-292-07) | 2026-08-19 | Active |
| 87063-0292-10 | 10 TABLET in 1 BOTTLE (87063-292-10) | 2026-08-19 | Active |
| 87063-0292-20 | 20 TABLET in 1 BOTTLE (87063-292-20) | 2026-08-19 | Active |
| 87063-0292-30 | 30 TABLET in 1 BOTTLE (87063-292-30) | 2026-08-19 | Active |
| 87063-0292-60 | 60 TABLET in 1 BOTTLE (87063-292-60) | 2026-08-19 | Active |
| 87063-0292-90 | 90 TABLET in 1 BOTTLE (87063-292-90) | 2026-08-19 | Active |
You're viewing the largest of 8 pack sizes for this product.
Pack size FAQ
What quantity is in NDC 87063-0292-01?
NDC 87063-0292-01 is a 100-count package — 100 tablet in 1 bottle.
What is the difference between NDC 87063-0292-01 and NDC 87063-0292-06?
Both are Nabumetone 750 mg Tablet — the drug itself is identical. NDC 87063-0292-01 is the 100-count package, while NDC 87063-0292-06 is the 6 tablets package.
What NDC number is used to bill for this package of Nabumetone 750 mg Tablet?
Bill NDC 87063-0292-01 — the 11-digit billing format is 87063029201. Pharmacy and medical claims use the 11-digit form; the FDA label may print a shorter form of the same code.
🧭 About this NDC listing & data coverage
Finished prescription product
What data is (and isn’t) available for this NDC — tap to expand
| NDC identity (package / product / labeler codes) | ✓ Available |
| Labeler | ✓ Available |
| Product & package description | ✓ Available |
| Marketing category & status | ✓ Available |
| Active ingredient / dosage form / route | ✓ Available |
| FDA label (SPL via DailyMed) | ✓ Available |
| Package photos | — Not published for this NDC No photo available yet for this listing. |
| Inactive ingredients (structured) | — Not published for this NDC The labeler did not submit a structured excipient list, or no SPL is available. |
| NADAC pharmacy acquisition price (CMS) | — Not published for this NDC CMS publishes NADAC only for NDCs reported in its retail-pharmacy survey. |
| Orange Book / therapeutic-equivalence data | ✓ Available |
| HCPCS J-code billing crosswalk | — Not published for this NDC Most self-administered / retail products have no J-code — that is normal. |
| Medicaid utilization (CMS SDUD) | — Not published for this NDC CMS reports utilization only for NDCs with Medicaid claims above its privacy threshold. |
“Not published” reflects what the public FDA / CMS / NLM sources provide for this exact package code — it is a property of the data feeds, not a judgment about the product.
Questions about this listing
Why is there no price listed?
The pricing shown on our NDC pages comes from CMS NADAC, a voluntary survey of retail community pharmacy invoices. CMS does not publish a NADAC for every NDC — packages outside the retail survey (institutional and hospital products, bulk packages, discontinued items, and many OTC items) may never receive one. A missing price reflects the survey's scope, not this product's actual cost, and does not mean the product is free or unavailable.
Is the NDC printed on the package the same as the 11-digit billing NDC?
Yes, they identify this exact package in different formats. The FDA registers it as 87063-292-01, which is what is printed on the packaging and shown on DailyMed. Insurance claims use a fixed 11-digit 5-4-2 format, so the short segment is padded with a leading zero: 87063-0292-01, written without dashes as 87063029201. The Identity section at the top of this page lists every form of this code.
What do the three segments of this NDC mean?
In 87063-0292-01, the first segment (87063) is the labeler code FDA assigned to ASCLEMED USA INC.; the middle segment (0292) identifies this specific product — its ingredient, strength, and dosage form; and the last segment (01) identifies this exact package size and type. Together they name one specific package of one specific product.
Is this package still being marketed?
Yes, per the latest FDA NDC Directory data on this page: this package is listed as actively marketed, with no marketing end date reported by ASCLEMED USA INC.. Listing status can change — the directory data on this page refreshes weekly.
Does this product come in other package sizes?
Yes — the FDA directory lists 7 other package presentations of this same product, including 6 tablets (87063-0292-06), 7 tablets (87063-0292-07), 10 tablets (87063-0292-10). Each has its own NDC and its own page — see the package list near the top of this page.
Who lists this product with the FDA?
ASCLEMED USA INC. is the labeler of record for this NDC — the company under whose FDA-assigned code the package is listed. The labeler may be the manufacturer itself or a distributor marketing the product under its own code.
Do I need a prescription for this product?
This NDC is listed with FDA as a prescription product, so it is dispensed under a prescriber's order. Your pharmacist can tell you whether any over-the-counter forms of the same medication exist.
This page identifies an FDA-listed package (the NDC) and reports public regulatory and pricing data about the listing. It is reference information, not a medical recommendation — talk to your pharmacist or prescriber about your own medication.
Where does this data come from?
Listing facts (marketing category, packager status, marketing dates) from the FDA openFDA NDC Directory; label availability from DailyMed; pricing coverage from CMS NADAC; equivalence scope from the FDA Orange Book.
📄 Full prescribing information FDA SPL
The complete FDA label for this product — the official prescribing information, verbatim, section by section. Jump with a chip, search within the label, or expand everything.
📄 FDA label ▾
No FDA label is on file for this product yet. Labels load from openFDA / DailyMed and refresh weekly.
No label section mentions that — try another word, or open the full label on DailyMed below.
Source: FDA Structured Product Labeling, mirrored from DailyMed / openFDA.
Prefer the government’s original formatting? View this label on DailyMed ↗
For educational and professional reference only — not medical advice. Pricing reflects published
NADAC and CMS ASP (free public data) and may differ from your acquisition cost; always verify before billing or dispensing.