NAPROXEN SODIUM TABLET [PHARMACY VALUE ALLIANCE, LLC]

NAPROXEN SODIUM TABLET [PHARMACY VALUE ALLIANCE, LLC]
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NDC 68016-660-05, 68016-660-10, 68016-660-24
Set ID 47932f2d-2fce-60d3-e054-00144ff88e88
Category HUMAN OTC DRUG LABEL
Packager Pharmacy Value Alliance, LLC
Generic Name
Product Class
Product Number
Application Number ANDA091353
  • Active Ingredient

    (in each caplet)

    Naproxen sodium 220 mg

    (naproxen 200 mg) (NSAID)**

    **nonsteroidal anti-inflammatory drug

  • Purposes

    Pain reliever/fever reducer

  • Uses

    ■ temporarily relieves minor aches and pains due to:

    ■ minor pain of arthritis

    ■ muscular aches

    ■ backache

    ■ menstrual cramps

    ■ headache

    ■ toothache

    ■ the common cold

    ■ temporarily reduces fever

  • 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.

  • Do not use

    ■ if you have ever had an allergic reaction to any other pain reliever/fever reducer

    ■ right before or after heart surgery

  • Ask a doctor before use if

    ■ the stomach bleeding warning applies to you

    ■ you have a history of stomach problems, such as heartburn

    ■ you have high blood pressure, heart disease, liver cirrhosis, kidney disease, asthma, or had a stroke

    ■ you are taking a diuretic

    ■ you have problems or serious side effects from taking pain relievers or fever reducers

  • Ask a doctor or pharmacist before use if you are

    ■ under a doctor’s care for any serious condition

    ■ taking any other drug

  • When using this product

    ■ take with food or milk if stomach upset occurs

  • Stop use and ask a doctor if

    ■ you experience any of the following signs of stomach bleeding:

    ■ feel faint

    ■ vomit blood

    ■ have bloody or black stools

    ■ have stomach pain that does not get better

    you have symptoms of heart problems or stroke:

    ■ chest pain

    ■ trouble breathing

    ■ weakness in one part or side of body

    ■ slurred speech

    ■ leg swelling

    ■ pain gets worse or lasts more than 10 days

    ■ fever gets worse or lasts more than 3 days

    ■ you have difficulty swallowing

    ■ it feels like the pill is stuck in your throat

    ■ redness or swelling is present in the painful area

    ■ any new symptoms appear

  • If pregnant or breast-feeding

    ask a health professional before use. It is especially important not to use naproxen sodium during the last 3 months of pregnancy unless definitely directed to do so by a doctor because it may cause problems in the unborn child or complications during delivery.

  • Keep out of reach of children

    In case of overdose, get medical help or contact a Poison Control Center right away.

  • 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 caplet every 8 to 12 hours while symptoms last

    ■ for the first dose you may take 2 caplets within the first hour

    ■ do not exceed 2 caplets in any 8- to 12- hour period

    ■ do not exceed 3 caplets in a 24- hour period

    Children under 12 years

    ■ ask a doctor

  • Other information

    ■ each caplet contains: sodium 20 mg

    ■ store at 20 - 25°C (68 to 77°F). Avoid high humidity and excessive heat above 40°C (104°F)

  • Inactive ingredients

    FD&C blue #2 aluminum lake, hypromellose 2910, maize starch, microcrystalline cellulose, polyethylene glycol, povidone k-30, sodium starch glycolate, stearic acid, titanium dioxide.

  • Questions or comments?

    1-877-770-3183 Mon-Fri 9:00 AM to 4:00 PM EST.

  • PRINCIPAL DISPLAY PANEL

    24 count

  • PRINCIPAL DISPLAY PANEL

    50 count

  • PRINCIPAL DISPLAY PANEL

    100 count

  • INGREDIENTS AND APPEARANCE
    NAPROXEN SODIUM 
    naproxen sodium tablet
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:68016-660
    Route of AdministrationORAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    NAPROXEN SODIUM (UNII: 9TN87S3A3C) (NAPROXEN - UNII:57Y76R9ATQ) NAPROXEN SODIUM220 mg
    Inactive Ingredients
    Ingredient NameStrength
    POLYETHYLENE GLYCOL, UNSPECIFIED (UNII: 3WJQ0SDW1A)  
    MICROCRYSTALLINE CELLULOSE (UNII: OP1R32D61U)  
    HYPROMELLOSES (UNII: 3NXW29V3WO)  
    STARCH, CORN (UNII: O8232NY3SJ)  
    TITANIUM DIOXIDE (UNII: 15FIX9V2JP)  
    POVIDONE K30 (UNII: U725QWY32X)  
    SODIUM STARCH GLYCOLATE TYPE A POTATO (UNII: 5856J3G2A2)  
    STEARIC ACID (UNII: 4ELV7Z65AP)  
    FD&C BLUE NO. 2 (UNII: L06K8R7DQK)  
    Product Characteristics
    ColorblueScoreno score
    ShapeOVALSize12mm
    FlavorImprint Code 220
    Contains    
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:68016-660-0550 in 1 BOTTLE; Type 0: Not a Combination Product02/25/2016
    2NDC:68016-660-10100 in 1 BOTTLE; Type 0: Not a Combination Product02/25/2016
    3NDC:68016-660-2424 in 1 BOTTLE; Type 0: Not a Combination Product02/01/2017
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    ANDAANDA09135302/25/2016
    Labeler - Pharmacy Value Alliance, LLC (101668460)
    Registrant - Granules USA, Inc (137098864)

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