Home › NDC Lookup › Ingredients › Naproxen Sodium › 71335-1282-09
Naproxen 220 mg Tablet, 24-count — NDC 71335-1282-09 package photo

Naproxen 220 mg Tablet, 24-count

by Bryant Ranch Prepack · 24 TABLET in 1 BOTTLE (71335-1282-9)
NDC 71335-1282-09
🏷️ FDA NDC (as labeled) 71335-1282-9 billing pads the package segment with a zero
This package
Contains24-count Pack sizes9 compare ↓
Also comes in: 14 tablets 71335-1282-06 20 tablets 71335-1282-01 30 tablets 71335-1282-02 40 tablets 71335-1282-03 50 tablets 71335-1282-04 60 tablets 71335-1282-05 90 tablets 71335-1282-08 100 tablets 71335-1282-07
OTC Generic 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) 71335-1282-9
Product NDC 71335-1282
11-digit billing NDC 71335128209
RxCUI 849574
UNII 9TN87S3A3C
Application # ANDA204872
SPL Set ID f9ddc614-26b7-48dc-ae93-02da6388f2d5
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 2019-01-01
Route ORAL
Dosage form TABLET
Substance NAPROXEN SODIUM
GPI-14 66100060100303
GPI class Naproxen Sodium
GCN Seq No 021980
GCN 47132
HICL code 003726
Ingredient (HICL) Naproxen Sodium
HIC1 code S
Therapeutic class — broad (HIC1) Locomotor System
HIC2 code S2
Therapeutic class — intermediate (HIC2) Drugs Acting Principally On Joints
HIC3 code S2B
Therapeutic class — specific (HIC3) Nsaids, Cyclooxygenase Inhibitor Type Analgesics
AHFS code 28:08.04.04
AHFS class Reversible Cox-1/Cox-2 Inhibitors
FDB label name NAPROXEN SODIUM 220 MG TABLET
FDB brand name Naproxen Sodium
Legend status O — Over-the-counter (OTC) drug or device
Why two NDCs? The FDA registers this code as 71335-1282-9 — 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 → 71335-1282-09. 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.

🏷️ RxNorm drug class

This medicine belongs to the Nonsteroidal Anti-inflammatory Drug class.

Pharmacologic class Nonsteroidal Anti-inflammatory Drug
Drug family (ATC) Propionic acid derivatives, Antiinflammatory products for vaginal administration, Antiinflammatory preparations, non-steroids for topical use
How it works Cyclooxygenase Inhibitors
Where does this data come from?
Therapeutic classes from RxNorm RxClass (U.S. National Library of Medicine) — Established Pharmacologic Class (FDA), ATC drug family (WHO) and mechanism of action, matched by this product’s RxCUI.

🏭 Manufacturer & labeler

LabelerBryant Ranch Prepack
Application holderLNK INTERNATIONAL INC
FDA applicationANDA204872 (ANDA)
Labeler code71335
First marketedJan 2019
Product typeHuman Otc Drug
Portfolio4,433 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

Label name NAPROXEN SODIUM 220 MG TABLET Ingredient Naproxen Sodium
📖 What it is MedlinePlus · NLM

Prescription naproxen is used to relieve pain, tenderness, swelling, and stiffness caused by osteoarthritis (arthritis caused by a breakdown of the lining of the joints), rheumatoid arthritis (arthritis caused by swelling of the lining of the joints), juvenile arthritis (a form of joint disease in children), and ankylosing spondylitis (arthritis that mainly affects the spine). Prescription naproxen tablets, extended-release tablets, and suspension are also used to relieve shoulder pain caused by bursitis (inflammation of a fluid-filled sac in the shoulder joint), tendinitis (inflammation of th...

Read the full MedlinePlus article ↗
📗 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.

💊 What it looks like

Color blue
ShapeRound
Imprint44;417
Size1 mm
ScoringNot scored
One label can cover several strengths, so colors may be combined — always confirm a loose pill against the dispensed prescription label or a pharmacist.
Where does this data come from?
Physical description (imprint, shape, color, scoring, coating) from this product’s FDA Structured Product Labeling (SPL), mirrored from DailyMed / openFDA.

🧪 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.

💡 Tap an ingredient (hover on desktop) to see what it is and why it’s used.

  • UNII M28OL1HH48
    Croscarmellose sodium is a plant-based substance derived from cellulose. It acts as a disintegrant, helping tablets and capsules break down quickly in the digestive system so the medicine can be absorbed.
  • UNII L06K8R7DQK
    A synthetic blue dye approved by the FDA for use in medications and foods. It serves as a colorant to make pills and liquids visually distinct and easier to identify.
  • UNII 70097M6I30
    Magnesium stearate is a salt made from magnesium and stearic acid, a fatty substance. It's used in tablets and capsules as a lubricant and glidant to help ingredients flow smoothly during manufacturing and prevent sticking.
  • UNII OP1R32D61U
    Microcrystalline cellulose is a purified form of cellulose, a natural fiber from plant sources. It acts as a binder and filler in tablets and capsules, helping hold ingredients together and give the medicine its shape and size.
  • UNII 3WJQ0SDW1A
    Polyethylene glycol is a synthetic liquid or solid polymer used in medicines as a solvent, lubricant, and humectant. It helps dissolve active ingredients, reduces friction during manufacturing, and retains moisture in the final product.
  • UNII 532B59J990
    Polyvinyl alcohol is a synthetic polymer made from plant-derived materials. It's used as a binder to hold ingredients together, a film-former in coatings, and a thickener in liquid formulations.
  • UNII FZ989GH94E
    Povidone is a synthetic polymer made from a plastic-like material. It acts as a binder to hold tablet ingredients together and as a disintegrant to help the tablet break apart in your stomach so the medicine can be absorbed.
  • UNII ETJ7Z6XBU4
    Silicon dioxide is a naturally occurring mineral used as a glidant and anti-caking agent. It helps powder ingredients flow smoothly and prevents clumping during manufacturing and storage.
  • UNII 7SEV7J4R1U
    A powder made from a naturally occurring mineral. In medicines, talc works as a glidant and anti-caking agent, helping tablets and capsules flow smoothly during manufacturing and preventing clumping.
  • UNII 15FIX9V2JP
    Titanium dioxide is a bright white mineral powder commonly used as a colorant and opacifying agent. It makes pills and tablets white or lighter in color and helps make coatings non-transparent.

10 inactive ingredients listed in the exact product block matched to this NDC.

The official label also statescroscarmellose sodium, FD&C blue #2 aluminum lake, magnesium stearate, microcrystalline cellulose, polyethylene glycol, polyvinyl alcohol, povidone, silicon dioxide, talc, titanium dioxide

Label-section wording can be broader than the structured product block and may mention additional formulation ingredients.

Where does this data come from?
Data sourced from official FDA Structured Product Labeling (SPL) via DailyMed — ingredient classCode="IACT" elements from the exact product block matched by this NDC. Label-section narrative from DailyMed / the openFDA label index is shown separately when available.

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 eachPer 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.
Try another pack size: 14 tablets 20 tablets 30 tablets 40 tablets 50 tablets 60 tablets 90 tablets 100 tablets
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 45802-0490-71 Padagis 50 tablets $0.059 — Discontinued —
Leader All Day Pain Relief 220 mg 70000-0171-01 Cardinal 100 tablets $0.059 — Discontinued —
Rugby All Day Relief 220 mg 00536-1093-01 Rugby 100 tablets $0.063 — Discontinued —
rugby all day relief 220 mg 00536-1094-01 Rugby 100 tablets $0.065 — Discontinued —
Naproxen Sodium 220 mg 63868-0465-01 Chain 100 tablets $0.065 — FDA listed —
Good Sense Naproxen Sodium 220 mg 00113-0901-62 L. 24 tablets $0.067 — Availability likely —
Good Sense Naproxen Sodium 220 mg 00113-4368-62 L. 24 tablets $0.067 — Availability likely —
Naproxen 220 mg 46122-0562-71 Amerisource 50 tablets $0.067 — Availability likely —
Naproxen 220 mg 46122-0564-71 Amerisource 50 tablets $0.067 — Availability likely —
Naproxen sodium 220 mg 69230-0329-01 Camber 100 tablets $0.067 — Availability likely —
Leader All Day Pain Relief 220 mg 70000-0201-02 Cardinal 50 tablets $0.067 — Availability likely —
foster and thrive all day pain relief 220 mg 70677-1137-01 Strategic 50 tablets $0.067 — Availability likely —
good sense naproxen sodium 220 mg 00113-1412-71 L. 50 tablets — — FDA listed —
Aleve Headache Pain 220 mg 00280-0041-01 Bayer 175 tablets — — FDA listed —
Aleve Back and Muscle Pain 220 mg 00280-0111-01 Bayer 10 tablets — — FDA listed —
Aleve Headache Pain 220 mg 00280-0112-01 Bayer 175 tablets — — FDA listed —
Aleve 220 mg 00280-0113-01 Bayer 10 tablets — — FDA listed —
Aleve Caplets 220 mg 00280-0114-01 Bayer 200 tablets — — FDA listed —
Aleve Caplets Soft Grip Arthritis 220 mg 00280-0115-01 Bayer 270 tablets — — FDA listed —
Aleve Caplets Easy Open Arthritis 220 mg 00280-0130-01 Bayer 90 tablets — — FDA listed —
Aleve Easy Open Arthritis 220 mg 00280-0131-01 Bayer 200 tablets — — FDA listed —
Aleve Caplets 220 mg 00280-6000-01 Bayer 24 tablets — — FDA listed —
Aleve 220 mg 00280-6010-01 Bayer 100 tablets — — FDA listed —
Aleve Gelcaps 220 mg 00280-6020-02 Bayer 90 tablets — — FDA listed —
Aleve Caplets - Easy Open Arthritis Cap 220 mg 00280-6050-01 Bayer 100 tablets — — FDA listed —
Aleve Easy Open Arthritis Cap 220 mg 00280-6060-20 Bayer 200 tablets — — FDA listed —
Aleve Gelcaps 220 mg 00280-6070-40 Bayer 40 tablets — — FDA listed —
Aleve Back and Muscle Pain 220 mg 00280-6092-02 Bayer 130 tablets — — FDA listed —
Aleve Headache Pain 220 mg 00280-8252-10 Bayer 10 tablets — — FDA listed —
All Day Pain Relief 220 mg 00363-0368-61 Walgreen 600 tablets — — Discontinued —
all day pain relief 200 mg 00363-0938-82 Walgreen 200 tablets — — FDA listed —
All Day Pain Relief 220 mg 00363-6099-01 WALGREENS 100 tablets — — FDA listed —
All Day Pain Relief 220 mg 00363-9608-01 WALGREENS 100 tablets — — FDA listed —
Back And Muscle Pain 220 mg 00363-9609-01 WALGREENS 100 tablets — — FDA listed —
Bayer Aleve 220 mg 00924-6000-00 Acme 1 tablet — — FDA listed —
up and up naproxen sodium 220 mg 11673-0368-71 Target 50 tablets — — FDA listed —
Naproxen Sodium 220 mg 11673-0764-05 TARGET 50 tablets — — FDA listed —
up and up naproxen sodium 220 mg 11673-0909-75 Target 90 tablets — — FDA listed —
Back and Muscle Pain 220 mg 11822-4170-02 Rite 100 tablets — — Discontinued —
Naproxen Sodium 220 mg 11822-4171-02 Rite 100 tablets — — Discontinued —
Naproxen Sodium 220 mg 11822-6040-02 Rite 100 tablets — — Discontinued —
Naproxen Sodium 220 mg 21130-0061-05 Safeway, 50 tablets — — FDA listed —
Naproxen 220 mg 21130-0062-05 Safeway, 50 tablets — — FDA listed —
signature care naproxen sodium 220 mg 21130-0180-62 Safeway 24 tablets — — Discontinued —
Naproxen Sodium 220 mg 21130-0593-79 Safeway 400 tablets — — FDA listed —
Pain Relief 220 mg 21130-0608-05 BETTER 50 tablets — — FDA listed —
Naproxen 220 mg 21130-0674-52 Better 90 tablets — — FDA listed —
Naproxen Sodium 220 mg 21130-0690-05 BETTER 50 tablets — — FDA listed —
Naproxen Sodium 220 mg 21130-0856-52 Better 90 tablets — — FDA listed —
Naproxen Sodium 220 mg 25000-0141-02 MARKSANS 3840 tablets — — FDA listed —
Naproxen Sodium 220 mg 25000-0144-02 MARKSANS 3840 tablets — — FDA listed —
Flanax 220 mg 27854-0160-00 Belmora 100 tablets — — Discontinued —
Flanax Menstrual Pain Reliever 220 mg 27854-0165-10 Belmora 10 tablets — — FDA listed —
AnaDent 220 mg 27854-0170-01 Belmora 24 tablets — — FDA listed —
Flanax Pain Reliever/Fever reducer 220 mg 27854-0505-01 Belmora 24 tablets — — FDA listed —
Belmora Flanax 220 mg 27854-0555-01 Belmora 24 tablets — — FDA listed —
Flanax Pain Reliever/Fever Reducer 220 mg 27854-0700-01 Belmora 24 tablets — — FDA listed —
Ana-Dent PAIN RELIEF 220 mg 27854-0701-01 Belmora 24 tablets — — FDA listed —
Naproxen Sodium 220 mg 30142-0954-10 Kroger 100 tablets — — FDA listed —
Topcare All Day Pain Relief 220 mg 36800-0140-82 Topco 200 tablets — — FDA listed —
TopCare All Day Pain Relief 220 mg 36800-0368-62 Topco 24 tablets — — FDA listed —
Topcare All Day Pain Relief 220 mg 36800-0490-62 Topco 24 tablets — — FDA listed —
topcare back and muscle pain 220 mg 36800-0696-75 Topco 90 tablets — — FDA listed —
All Day Pain Relief 220 mg 37808-0068-24 H 24 tablets — — FDA listed —
naproxen sodium 220 mg 37808-0631-82 H 200 tablets — — FDA listed —
naproxen sodium 220 mg 37808-0652-62 H 24 tablets — — FDA listed —
naproxen sodium 220 mg 37808-0713-79 H 400 tablets — — FDA listed —
Naproxen Sodium 220 mg 37835-0594-01 Bi-Mart 100 tablets — — FDA listed —
equaline naproxen sodium 220 mg 41163-0511-62 United 24 tablets — — FDA listed —
equaline naproxen sodium 220 mg 41163-0707-71 United 50 tablets — — FDA listed —
Naproxen Sodium 220 mg 41226-0609-05 Kroger 50 tablets — — FDA listed —
naproxen sodium 220 mg 41250-0313-82 Meijer 200 tablets — — FDA listed —
Naproxen Sodium 220 mg 41250-0477-62 Meijer 24 tablets — — FDA listed —
Naproxen Sodium 220 mg 41250-0680-71 Meijer 50 tablets — — FDA listed —
naproxen sodium 220 mg 41250-0818-62 Meijer 24 tablets — — FDA listed —
Care One Naproxen Sodium 220 mg 41520-0349-82 American 200 tablets — — FDA listed —
CareOne Naproxen Sodium 220 mg 41520-0507-48 American 90 tablets — — Discontinued —
Care One Naproxen Sodium 220 mg 41520-0533-71 American 50 tablets — — FDA listed —
Naproxen Sodium 220 mg 42507-0245-01 HYVEE 24 tablets — — FDA listed —
Naproxen Sodium 220 mg 42507-0844-01 HYVEE 24 tablets — — FDA listed —
First Aid Direct All Day Pain Relief 220 mg 42961-0122-02 Cintas 1 tablet — — FDA listed —
Naproxen Sodium 220 mg 43063-0909-20 PD-Rx 20 tablets — — FDA listed —
Naproxen Sodium Caplets 220 mg 43598-0058-29 Dr 200 tablets — — FDA listed —
Naproxen Sodium Headache Pain Caplets 220 mg 43598-0059-52 Dr.Reddy's 225 tablets — — FDA listed —
Naproxen Sodium Back and Muscle Pain Caplets 220 mg 43598-0060-52 Dr.Reddy's 225 tablets — — FDA listed —
Naproxen Sodium Headache Pain 220 mg 43598-0072-01 Dr.Reddy's 100 tablets — — FDA listed —
Naproxen Sodium Back and Muscle Pain 220 mg 43598-0074-01 Dr.Reddy's 100 tablets — — FDA listed —
Belmora Flanax 220 mg 47682-0037-50 Unifirst 1 tablet — — FDA listed —
Medique Mediproxen 220 mg 47682-0237-33 Unifirst 1 tablet — — FDA listed —
Bayer Aleve 220 mg 47682-0488-50 Unifirst 50 tablets — — FDA listed —
Medique at Home Mediproxen 220 mg 47682-0737-50 Unifirst 1 tablet — — FDA listed —
Calmadol Pain Reliever 220 mg 48201-0007-24 GRANDALL 24 tablets — — FDA listed —
Naproxen Sodium 220 mg 49483-0608-00 TIME 6500 tablets — — FDA listed —
Naproxen Sodium 220 mg 49483-0609-00 TIME 6500 tablets — — FDA listed —
Naproxen Sodium 220 mg 50090-0685-01 A-S 10 tablets — — FDA listed —
Medique Mediproxen 220 mg 50090-2388-00 A-S 1 tablet — — FDA listed —
rugby all day relief 220 mg 50090-3356-00 A-S 30 tablets — — FDA listed —
Naproxen 220 mg 50844-0261-08 L.N.K. 24 tablets — — FDA listed —
Naproxen Sodium 220 mg 50844-0417-14 L.N.K. 500 tablets — — FDA listed —
Naproxen Headache Pain 220 mg 50844-0471-14 L.N.K. 500 tablets — — FDA listed —
Naproxen Sodium 220 mg 50844-0604-09 L.N.K. 5 tablets — — FDA listed —
Naproxen Back and Muscle Pain 220 mg 50844-0714-14 L.N.K. 500 tablets — — FDA listed —
Naproxen Sodium 220 mg 51316-0608-90 CVS 90 tablets — — FDA listed —
Naproxen Sodium 220 mg 51316-0761-20 CVS 200 tablets — — FDA listed —
Naproxen Sodium 220 mg 51316-0762-70 CVS 270 tablets — — FDA listed —
Back and Muscle Pain 220 mg 51316-0817-08 CVS 24 tablets — — FDA listed —
CAREALL Naproxen 220 mg 51824-0072-01 New 100 tablets — — FDA listed —
CAREALL Naproxen Sodium 220 mg 51824-0109-01 New 100 tablets — — FDA listed —
Naproxen Sodium 220mg 220 mg 53185-0394-50 Athlete's 50 tablets — — FDA listed —
Naproxen Sodium 220 mg 53185-0604-12 Athlete's 100 tablets — — FDA listed —
Naproxen Sodium 220mg 220 mg 53329-0688-30 Medline 100 tablets — — Discontinued —
Naproxen Sodium (NSAID) Fever Reducer/ Pain Reliever 220 mg 53746-0191-05 Amneal 500 tablets — — FDA listed —
Naproxen Sodium (NSAID) Fever Reducer/ Pain Reliever 220 mg 53746-0192-05 Amneal 500 tablets — — FDA listed —
Naproxen 220 mg 53943-0144-02 DISCOUNT 50 tablets — — FDA listed —
Naproxen 220 mg 53943-0145-02 DISCOUNT 50 tablets — — FDA listed —
Naproxen Sodium 220 mg 55111-0272-01 Dr.Reddy's 100 tablets — — FDA listed —
Naproxen Sodium 220 mg 55111-0273-01 Dr. 100 tablets — — FDA listed —
exchange select naproxen sodium 220 mg 55301-0368-71 Army 50 tablets — — FDA listed —
Naproxen 220 mg 55319-0406-52 Family 90 tablets — — Discontinued —
Naproxen 220 mg 55319-0717-08 Family 24 tablets — — FDA listed —
Rapidol Naproxen 220 mg 55758-0048-24 Pharmadel 24 tablets — — FDA listed —
DG Health Naproxen Sodium 220 mg 55910-0481-62 Dolgencorp 24 tablets — — FDA listed —
DG Health Naproxen Sodium 220 mg 55910-0490-62 Dolgencorp 24 tablets — — FDA listed —
dg health naproxen sodium 220 mg 55910-0500-71 Dolgencorp 50 tablets — — Discontinued —
dg health naproxen sodium 220 mg 55910-0729-62 Dolgencorp 24 tablets — — FDA listed —
All Day Relief 220 mg 56062-0368-62 Publix 24 tablets — — FDA listed —
all day relief 220 mg 56062-0490-71 Publix 50 tablets — — FDA listed —
Naproxen Sodium 220 mg 57344-0145-01 AAA 24 tablets — — FDA listed —
Naproxen 220 mg 57896-0954-01 Geri-Care 100 tablets — — FDA listed —
Naproxen Sodium HEADACHE PAIN 220 mg 58602-0735-07 Aurohealth 24 tablets — — FDA listed —
Naproxen Sodium BACK AND MUSCLE PAIN 220 mg 58602-0736-07 Aurohealth 24 tablets — — FDA listed —
Naproxen Sodium HEADACHE PAIN 220 mg 58602-0737-07 Aurohealth 24 tablets — — FDA listed —
Naproxen Sodium 220 mg 58602-0738-07 Aurohealth 24 tablets — — FDA listed —
Naproxen Sodium BACK AND MUSCLE PAIN 220 mg 58602-0739-07 Aurohealth 24 tablets — — FDA listed —
Naproxen Sodium 220 mg 58602-0819-07 Aurohealth 24 tablets — — FDA listed —
Naproxen Sodium 220 mg 58602-0845-21 Aurohealth 100 tablets — — FDA listed —
Artridol 220 mg 59428-0604-08 Zapotol 24 tablets — — FDA listed —
All Day Pain Relief 220 mg 59726-0169-15 P 15 tablets — — FDA listed —
naproxen sodium 220 mg 59779-0914-75 CVS 90 tablets — — FDA listed —
Naproxen Sodium 220 mg 61504-0145-02 AMERIFOODS 50 tablets — — FDA listed —
Naproxen Sodium 220 mg 62207-0327-41 Granules 24 tablets — — FDA listed —
Naproxen Sodium 220 mg 62207-0328-41 Granules 24 tablets — — FDA listed —
Naproxen Sodium 220 mg 62207-0728-24 Granules 24 tablets — — FDA listed —
Naproxen Sodium 220 mg 62207-0729-24 Granules 24 tablets — — FDA listed —
Naproxen Sodium 220 mg 62207-0761-42 Granules 50 tablets — — FDA listed —
Naproxen Sodium 220 mg 62207-0762-42 Granules 50 tablets — — FDA listed —
Naproxen Sodium 220 mg 63187-0596-24 Proficient 24 tablets — — FDA listed —
Good Sense Naproxen Sodium 220 mg 63187-0794-20 Proficient 20 tablets — — FDA listed —
Naproxen Sodium 220 mg 63868-0466-01 Chain 100 tablets — — FDA listed —
All Day Pain Relief 220 mg 63941-0144-01 VALU 24 tablets — — FDA listed —
All Day Pain Relief 220 mg 63941-0245-01 VALU 24 tablets — — FDA listed —
Naproxen Sodium 220 mg 63941-0444-01 VALU 24 tablets — — FDA listed —
Naproxen Sodium 220 mg 63941-0445-01 VALU 24 tablets — — FDA listed —
kirkland signature naproxen sodium 220 mg 63981-0368-79 Costco 400 tablets — — FDA listed —
Aleve 220 mg 66715-5103-00 Lil' 60 tablets — — FDA listed —
24/7 Life by 7-Eleven Naproxen Sodium 220 mg 66715-5428-04 Lil' 24 tablets — — FDA listed —
Aleve 220 mg 66715-6402-08 Lil' 30 tablets — — FDA listed —
Aleve, TRAVEL BASIX 220 mg 66715-6411-02 Lil' 2 tablets — — FDA listed —
Aleve 220 mg 66715-6502-02 Lil' 2 tablets — — FDA listed —
Aleve 220 mg 66715-9702-01 Lil' 1 tablet — — Discontinued —
Lil Drug Store Pain Relief All Day 220 mg 66715-9740-04 Lil' 12 tablets — — FDA listed —
Naproxen Sodium 220 mg 67091-0138-50 WinCo 50 tablets — — FDA listed —
Naproxen Sodium 220 mg 67091-0140-10 WinCo 100 tablets — — FDA listed —
Flanax Pain Reliever/Fever Reducer 220 mg 67751-0125-01 Navajo 2 tablets — — FDA listed —
Aleve 220 mg 67751-0144-03 Navajo 1 tablet — — FDA listed —
Naproxen 220 mg 68071-5039-01 NuCare 21 tablets — — FDA listed —
Naproxen Sodium 220 mg 68196-0255-20 SAM'S 400 tablets — — FDA listed —
Berkley and Jensen Naproxen Sodium 220 mg 68391-0368-79 BJWC 400 tablets — — FDA listed —
Naproxen 220 mg 68788-7572-02 Preferred 20 tablets — — FDA listed —
Good Sense Naproxen Sodium 220 mg 68788-8443-02 Preferred 20 tablets — — FDA listed —
Naproxen Sodium 220 mg 68998-0144-03 Marc 100 tablets — — FDA listed —
Naproxen Sodium 220 mg 68998-0145-03 Marc 100 tablets — — FDA listed —
Naproxen Caplets All day relief for pain 220 mg 69168-0362-07 Allegiant 10 tablets — — FDA listed —
Naproxen Caplets 220 mg 69168-0394-24 Allegiant 24 tablets — — FDA listed —
Naproxen Sodium 220mg 220 mg 69168-0395-17 Allegiant 300 tablets — — FDA listed —
Naproxen Sodium 220mg 220 mg 69197-0394-24 Command 24 tablets — — FDA listed —
All Day Pain Relief 220 mg 69517-0109-02 HealthLife 32 tablets — — FDA listed —
Proxen Np 660 220 mg 69729-0123-12 OPMX 12 tablets — — FDA listed —
Naproxen Sodium 220 mg 69842-0811-62 CVS 24 tablets — — FDA listed —
Naproxen Sodium 220 mg 69848-0010-01 Granules 10 tablets — — FDA listed —
Aleve 220 mg 70264-0011-01 R 50 tablets — — FDA listed —
Naproxen Sodium 220 mg 71141-0182-32 Lidl 100 tablets — — FDA listed —
Naproxen 220 mg 71205-0595-30 Proficient 30 tablets — — FDA listed —
Naproxen Sodium 220 mg 71335-1061-01 Bryant 20 tablets — — FDA listed —
Naproxen 220 mgthis 71335-1282-09 Bryant 24 tablets — — FDA listed —
Good Sense Naproxen Sodium 220 mg 71335-2584-01 Bryant 20 tablets — — FDA listed —
Rugby All Day Relief 220 mg 71335-3009-01 Bryant 20 tablets — — FDA listed —
Naproxen Sodium 220 mg 72036-0144-01 Harris 24 tablets — — FDA listed —
Naproxen Sodium 220 mg 72036-0145-01 Harris 24 tablets — — FDA listed —
Basic Care Naproxen Sodium 220 mg 72288-0331-62 Amazon.com 24 tablets — — Discontinued —
Amazon Basic Care Naproxen Sodium 220 mg 72288-0366-20 Amazon.com 200 tablets — — FDA listed —
basic care naproxen sodium 220 mg 72288-0368-75 Amazon.com 90 tablets — — FDA listed —
Basic Care Naproxen Sodium 220 mg 72288-0489-75 Amazon.com 90 tablets — — FDA listed —
Naproxen Sodium 220 mg 72789-0543-14 PD-Rx 14 tablets — — FDA listed —
All Day Pain Relief 220 mg 79903-0005-10 WALMART 40 tablets — — Discontinued —
Naproxen Sodium 220 mg 79903-0231-50 WALMART 50 tablets — — FDA listed —
Naproxen Sodium 220 mg 79903-0232-90 WALMART 90 tablets — — FDA listed —
All Day Pain Relief 220 mg 79903-0389-50 Walmart 50 tablets — — FDA listed —
All Day Back and Muscle Pain Relief 220 mg 79903-0609-09 Walmart 90 tablets — — FDA listed —
betr headache pain relief 220 mg 80267-0001-71 Live 50 tablets — — FDA listed —
Naproxen Sodium 220 mg 81522-0045-05 FSA 200 tablets — — FDA listed —
Pain Relief 220 mg 82501-1576-01 Gobrands, 100 tablets — — FDA listed —
Naproxen Sodium 220 mg 83324-0108-01 CHAIN 100 tablets — — FDA listed —
Naproxen Sodium 220 mg 83324-0109-01 CHAIN 100 tablets — — FDA listed —
Aleve Caplets 220 mg 85237-1832-01 Select 1 tablet — — FDA listed —
Medique Mediproxen 220 mg 85766-0121-01 Sportpharm 1 tablet — — FDA listed —
Dr Simi All Day Pain Relief 220 mg 85786-0104-24 Farmacias 24 tablets — — FDA listed —
Naproxen Sodium 220mg 220 mg 85828-0394-92 Grocery 90 tablets — — FDA listed —
Naproxen Sodium 220 mg 00363-7510-20 Walgreens 20 tablets — — FDA listed —
Naproxen Sodium Headache Pain 220 mg 43598-0071-01 Dr.Reddy's 100 tablets — — FDA listed —
Naproxen Sodium Back and Muscle Pain 220 mg 43598-0073-01 Dr.Reddy's 100 tablets — — 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
Jan 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 Naproxen — the program that covers self-administered drugs. 17 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. 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
$5.99M
Claims incl. refills
655K
Beneficiaries
478.5K
Spend / beneficiary
$12.52
Spend / claim
$9.15
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 NAPROXEN (this brand).

Top reported reactions

Pain10,415
Fatigue9,349
Arthralgia8,826
Nausea8,541
Headache7,237
Diarrhoea6,972
Vomiting6,343

Age at onset

Neonate142
Infant19
Child213
Adolescent345
Adult10,364
Elderly3,280

Reporter sex

88,851 reports
Male · 32%
Female · 68%
Unknown · 0%

Serious outcomes

Hospitalization30,080
Reports over time (by year) — tap or hover for the count & year
2019 2021 2023 2026 7,747 0
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 NDCDescription Marketing startStatus
71335-1282-01 20 TABLET in 1 BOTTLE (71335-1282-1) 2022-02-23 Active
71335-1282-02 30 TABLET in 1 BOTTLE (71335-1282-2) 2022-02-23 Active
71335-1282-03 40 TABLET in 1 BOTTLE (71335-1282-3) 2022-02-23 Active
71335-1282-04 50 TABLET in 1 BOTTLE (71335-1282-4) 2022-02-23 Active
71335-1282-05 60 TABLET in 1 BOTTLE (71335-1282-5) 2022-02-23 Active
71335-1282-06 14 TABLET in 1 BOTTLE (71335-1282-6) 2022-02-23 Active
71335-1282-07 100 TABLET in 1 BOTTLE (71335-1282-7) 2022-02-23 Active
71335-1282-08 90 TABLET in 1 BOTTLE (71335-1282-8) 2022-02-23 Active
71335-1282-09 You're viewing this 24 TABLET in 1 BOTTLE (71335-1282-9) 2022-02-23 Active

You're viewing one of 9 pack sizes for this product.

Pack size FAQ

What quantity is in NDC 71335-1282-09?
NDC 71335-1282-09 is a 24-count package — 24 tablet in 1 bottle.
What is the difference between NDC 71335-1282-09 and NDC 71335-1282-06?
Both are Naproxen 220 mg Tablet — the drug itself is identical. NDC 71335-1282-09 is the 24-count package, while NDC 71335-1282-06 is the 14 tablets package.
What NDC number is used to bill for this package of Naproxen 220 mg Tablet?
Bill NDC 71335-1282-09 — the 11-digit billing format is 71335128209. 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

Over-the-counter (OTC) 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 ✓ Available
Inactive ingredients (structured) ✓ 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

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 71335-1282-9, 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: 71335-1282-09, written without dashes as 71335128209. 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 71335-1282-09, the first segment (71335) is the labeler code FDA assigned to Bryant Ranch Prepack; the middle segment (1282) identifies this specific product — its ingredient, strength, and dosage form; and the last segment (09) 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 Bryant Ranch Prepack. 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 8 other package presentations of this same product, including 14 tablets (71335-1282-06), 20 tablets (71335-1282-01), 30 tablets (71335-1282-02). 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?
Bryant Ranch Prepack 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 an over-the-counter product, so it does not require a prescription. Follow the package directions, and ask your pharmacist if you are unsure whether it is right for you.
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.

📄 FDA label — Drug Facts FDA SPL

The complete FDA label for this product — the official Drug Facts labeling, verbatim, section by section. Jump with a chip, search within the label, or expand everything.
🎯 Indications and Usage ⏱️ Dosage and Administration ⚠️ Warnings 📦 How Supplied / Storage and Handling 📦 Storage and Handling 🧪 Active Ingredient 🧪 Inactive Ingredients 🎯 Purpose
🎯 Indications and Usage 26 words ▾

Uses temporarily relieves minor aches and pain due to: backache muscular aches minor pain of arthritis menstrual cramps headache toothache the common cold temporarily reduces fever

⏱️ Dosage and Administration 83 words ▾

Directions do not take more than directed the smallest effective dose should be used drink a full glass of water with each dose adults and children 12 years and older take 1 tablet every 8 to 12 hours while symptoms last for the first dose you may take 2 tablets within the first hour do not exceed 2 tablets in any 8 to 12 hour period do not exceed 3 tablets in a 24 hour period children under 12 years: ask a doctor

⚠️ Warnings 154 words ▾

Warnings Allergy alert: Naproxen sodium may cause a severe allergic reaction, especially in people allergic to aspirin. Symptoms may include: hives facial swelling asthma (wheezing) shock skin reddening rash blisters If an allergic reaction occurs, stop use and seek medical help right away. Stomach bleeding warning: This product contains an NSAID, which may cause severe stomach bleeding.

The chance is higher if you: are age 60 or older have had stomach ulcers or bleeding problems take a blood thinning (anticoagulant) or steroid drug take other drugs containing prescription or nonprescription NSAIDs (aspirin, ibuprofen, naproxen, or others) have 3 or more alcoholic drinks every day while using this product. take more or for a longer time than directed. Heart attack and stroke warning: NSAIDs, except aspirin, increase the risk of heart attack, heart failure, and stroke. These can be fatal.

The risk is higher if you use more than directed or for longer than directed.

📦 How Supplied / Storage and Handling 79 words ▾

HOW SUPPLIED Naproxen Sodium 220 mg Tablet NDC 71335-1282-1: 20 Tablets in a BOTTLE NDC 71335-1282-2: 30 Tablets in a BOTTLE NDC 71335-1282-3: 40 Tablets in a BOTTLE NDC 71335-1282-4: 50 Tablets in a BOTTLE NDC 71335-1282-5: 60 Tablets in a BOTTLE NDC 71335-1282-6: 14 Tablets in a BOTTLE NDC 71335-1282-7: 100 Tablets in a BOTTLE NDC 71335-1282-8: 90 Tablets in a BOTTLE NDC 71335-1282-9: 24 Tablets in a BOTTLE Repackaged/Relabeled by: Bryant Ranch Prepack, Inc. Burbank, CA 91504

📦 Storage and Handling 22 words ▾

Storage Store at 20-25 o C (68-77 o F). Avoid high humidity and excessive heat above 40 0 C (104 0 F)

🧪 Active Ingredient 16 words ▾

Active ingredient (in each tablet) Naproxen sodium 220 mg (Naproxen 200 mg) (NSAID)* *nonsteroidal anti-inflammatory drug

🧪 Inactive Ingredients 23 words ▾

Inactive ingredients croscarmellose sodium, FD&C blue #2 aluminum lake, magnesium stearate, microcrystalline cellulose, polyethylene glycol, polyvinyl alcohol, povidone, silicon dioxide, talc, titanium dioxide

🎯 Purpose 5 words ▾

Purpose Pain reliever/ fever reducer

Source: FDA Structured Product Labeling, mirrored from DailyMed / openFDA. Prefer the government’s original formatting? View this label on DailyMed ↗
← 71335-1278-00 · Bryant 71335-1286-01 · Bryant →
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.