Home › NDC Lookup › Ingredients › Naproxen Sodium › 10888-5015-00
💊image loading
(from DailyMed)

NAPROXEN SODIUM 220 mg Capsule, Liquid Filled, 6,000-count

by Patheon Softgels Inc · 6000 CAPSULE, LIQUID FILLED in 1 CONTAINER (10888-5015-0)
NDC 10888-5015-00
🏷️ FDA NDC (as labeled) 10888-5015-0 billing pads the package segment with a zero
On market Non-controlled
🗂️ Data synced Jul 24, 2026 · sources: openFDA · FDA label (DailyMed) · FDA Orange & Purple Book · First Databank · CMS NADAC, ASP, Medicare & Medicaid · RxNorm
📋 All sources & update times →

This page is curated, coded, and maintained by

Compiled from public FDA, CMS, DailyMed, NADAC, and related drug data sources. Editorial policy

⚠️
Other active recalls for Naproxen Sodium (different manufacturers) — 2 · tap to view
These affect other manufacturers’ products for the same ingredient — not necessarily the exact NDC on this page.
Class II · Mar 13, 2025 — CGMP Deviations (Glenmark Pharmaceuticals Inc., USA) · FDA recall D-0346-2025
Class II · Nov 7, 2023 — Labeling: Label Mix-Up-Indomethacin bottles may be labeled as Naproxen (Glenmark Pharmaceuticals Inc., USA) · FDA recall D-0124-2024
Each entry is an official FDA enforcement report — look up any recall number in the FDA recall database ↗

🆔 Identity & classification

FDA NDC (as labeled) 10888-5015-0
Product NDC 10888-5015
11-digit billing NDC 10888501500
SPL Set ID 66394228-4e28-49c3-a2cf-681b48e855d9
DEA schedule Non-controlled
Marketing category DRUG FOR FURTHER PROCESSING
Marketing status On market
FDA listing status Listed (active directory)
Marketing start 2014-09-30
Dosage form CAPSULE, LIQUID FILLED
Substance NAPROXEN SODIUM
Why two NDCs? The FDA registers this code as 10888-5015-0 — a 5-4-1 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 package segment → 10888-5015-00. 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

LabelerPatheon Softgels Inc
Labeler code10888
First marketedSep 2014
Product typeDrug For Further Processing
Portfolio6 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
  • They're very similar — naproxen sodium is just the salt form of naproxen, and it dissolves in water more quickly. That means your body absorbs naproxen sodium a bit faster, so it t...
  • What's the difference between naproxen and naproxen sodium — are they the same thing?
  • You can take it either way, but taking it with food, milk, or a full glass of water is a good idea because it helps protect your stomach. Naproxen can irritate the lining of your s...
  • Can I take naproxen on an empty stomach, or do I need to eat first?
📖 Read our full Naproxen guide →
1
Nutrient depletion considerations

Naproxen Sodium may be associated with lower levels of 1 nutrient — worth a chat with your pharmacist, not a cause for alarm.

🧪 Full Naproxen Sodium nutrient depletion report →
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.

🧪 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.

Loading inactive ingredients from the official FDA label in the background. No external source is being called by this page request.
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 systemPer mLPer 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

ProductLabelerPackNADAC/unitTEStatusPrice vs. this
Naproxen Sodium 220 mg 70677-1148-01 Strategic 40 capsules $0.151 — Availability likely —
Naproxen Sodium 220 mg 46122-0780-64 AMERISOURCE 20 capsules $0.151 — Availability likely —
Naproxen Sodium 220 mg 62011-0369-01 Strategic 40 capsules $0.156 — FDA listed —
Naproxen Sodium 220 mg 00363-0177-11 WALGREEN 20 capsules — — FDA listed —
Naproxen Sodium 220 mg 41163-0079-15 SUPERVALU 40 capsules — — FDA listed —
Naproxen Sodium 220 mg 41520-0748-20 Care 20 capsules — — FDA listed —
Naproxen Sodium 220 mg 51013-0137-15 PuraCap 20 capsules — — FDA listed —
Naproxen Sodium 220 mg 53345-0042-01 Humanwell 5000 capsules — — FDA listed —
Naproxen Sodium 220 mg 53943-0179-11 DISCOUNT 20 capsules — — FDA listed —
Naproxen Sodium 220 mg 55910-0748-20 Dolgencorp, 20 capsules — — FDA listed —
Naproxen Sodium 220 mg 68016-0056-40 Premier 40 capsules — — FDA listed —
Naproxen Sodium 220 mg 00363-0102-15 WALGREEN 40 capsules — — FDA listed —
Naproxen Sodium 220 mg 11673-0748-18 TARGET 180 capsules — — FDA listed —
Naproxen Sodium 220 mg 11822-0788-04 Rite 40 capsules — — FDA listed —
Naproxen Sodium 220 mg 30142-0285-22 KROGER 120 capsules — — FDA listed —
Naproxen Sodium 220 mg 36800-0204-11 TOP 20 capsules — — FDA listed —
Naproxen Sodium 220 mg 37808-0049-15 HEB 40 capsules — — FDA listed —
Naproxen Sodium 220 mg 49035-0382-22 Wal-Mart 120 capsules — — FDA listed —
Naproxen Sodium 220 mg 63868-0830-20 CHAIN 20 capsules — — FDA listed —
Naproxen Sodium 220 mg 63941-0681-16 VALU 50 capsules — — FDA listed —
Naproxen Sodium 220 mg 69452-0179-22 Bionpharma 120 capsules — — FDA listed —
Naproxen Sodium 220 mg 55301-0748-20 AAFES/Your 20 capsules — — FDA listed —
Naproxen Sodium 220 mg 49035-0748-12 EQUATE 120 capsules — — FDA listed —
Naproxen Sodium 220 mg 59428-0748-20 Productos 20 capsules — — FDA listed —
naproxen sodium 220 mg 69452-0284-25 Bionpharma 180 capsules — — FDA listed —
Naproxen Sodium 220 mgthis 10888-5015-00 Patheon 6000 capsules — — FDA listed —
Naproxen Sodium 220 mg 21130-0948-11 Albertsons 20 capsules — — FDA listed —
All Day Relief 220 mg 56062-0748-40 Publix 40 capsules — — FDA listed —
Aleve 220 mg 00280-6080-01 Bayer 120 capsules — — FDA listed —
Aleve Easy Open Arthritis Cap 220 mg 00280-6091-80 Bayer 80 capsules — — FDA listed —
naproxen sodium 220 mg 69452-0259-22 Bionpharma 120 capsules — — Discontinued —
Naproxen Sodium 220 mg 72476-0748-20 Care 20 capsules — — FDA listed —
Naproxen Sodium 220 mg 21130-0748-20 Safeway, 20 capsules — — FDA listed —
Naproxen Sodium 220 mg 41250-0225-15 MEIJER 40 capsules — — FDA listed —
Naproxen Sodium 220 mg 10888-8115-01 Patheon 6000 capsules — — FDA listed —
Naproxen Sodium 220 mg 49588-0003-01 Catalent 6000 capsules — — FDA listed —
Naproxen Sodium 220 mg 59726-0174-20 P 20 capsules — — FDA listed —
Naproxen Sodium 220 mg 59726-0751-20 P 20 capsules — — FDA listed —
Naproxen Sodium 220 mg 69842-0748-08 CVS 80 capsules — — FDA listed —
Naproxen Sodium 220 mg 10888-8130-01 Patheon 6000 capsules — — FDA listed —
Naproxen Sodium 220 mg 11673-0651-78 TARGET 80 capsules — — FDA listed —
Naproxen Sodium 220 mg 10888-8227-01 Patheon 6000 capsules — — FDA listed —
Naproxen Sodium 220 mg 10888-8271-01 Patheon 6000 capsules — — FDA listed —
Aleve liquid gels 220 mg 00280-0105-02 Bayer 160 capsules — — FDA listed —
Naproxen Sodium 220 mg 00363-0748-08 Walgreens 80 capsules — — FDA listed —
Naproxen Sodium 220 mg 10888-8129-01 Patheon 6000 capsules — — FDA listed —
Naproxen Sodium 220 mg 10888-8270-01 Patheon 6000 capsules — — FDA listed —
Naproxen Sodium 220 mg 59428-0784-20 Productos 20 capsules — — FDA listed —
Naproxen Sodium 220 mg 72288-0312-25 Amazon.com 180 capsules — — FDA listed —
About this product: other versions of the same ingredient, strength and form are listed above, least expensive first, with FDA equivalence ratings where available.
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

🏛️
2014
On the market since
Sep 2014
📍
2026
Currently FDA-listed
12 years listed
🔓
·
Generic versions listed
see equivalents
✅Generic appears available

FDA-approved generic versions are listed, and recent pricing/market data suggests they may be available — see Therapeutic equivalents.

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 Naproxen Sodium (matched by generic name) — the program that covers self-administered drugs. 4 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 Naproxen Sodium. CMS lists 4 products for this generic; we show the highest-spend one. 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
$441.8K
Claims incl. refills
15.2K
Beneficiaries
11.4K
Spend / beneficiary
$38.70
Spend / claim
$29.13
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.

📦 Packaging — all sizes for this product

Package NDCDescription Marketing startStatus
10888-5015-00 You're viewing this 6000 CAPSULE, LIQUID FILLED in 1 CONTAINER (10888-5015-0) — Active

🧭 About this NDC listing & data coverage

Listed for further processing / repackaging

What "drug for further processing" means

FDA lists this package under the "drug for further processing" marketing category: Patheon Softgels Inc supplies it to other companies for further processing or repackaging (blister cards that are later repackaged or co-packaged are a common example). The units themselves are a finished dosage form — which is why pricing or Medicaid data can still appear — but this exact package code may not be the presentation a retail pharmacy dispenses.

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 — Not published for this NDC Applies only to products approved under an NDA/ANDA; many listings are out of scope.
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

Is this NDC FDA-approved?
An NDC listing does not by itself establish FDA approval — the NDC Directory records that a product is listed with FDA, not that it was reviewed and approved. This listing's marketing category is "Drug For Further Processing". Products approved under an application carry an NDA, ANDA, or BLA number.
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 10888-5015-0, 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: 10888-5015-00, written without dashes as 10888501500. 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 10888-5015-00, the first segment (10888) is the labeler code FDA assigned to Patheon Softgels Inc; the middle segment (5015) identifies this specific product — its ingredient, strength, and dosage form; and the last segment (00) 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 Patheon Softgels Inc. Listing status can change — the directory data on this page refreshes weekly.
Who lists this product with the FDA?
Patheon Softgels 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.
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 FDA label FDA SPL

The complete FDA label for this product, verbatim, section by section. Jump with a chip, search within the label, or expand everything.
📄 FDA label
📄 FDA label 19 words ▾

No FDA label is on file for this product yet. Labels load from openFDA / DailyMed and refresh weekly.

Source: FDA Structured Product Labeling, mirrored from DailyMed / openFDA. Prefer the government’s original formatting? View this label on DailyMed ↗
← 10888-5014-01 · Patheon 10888-5022-01 · Patheon →
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.