Label: NAPROXEN SODIUM tablet

  • Category: HUMAN PRESCRIPTION DRUG LABEL
  • DEA Schedule: None
  • Marketing Status: Abbreviated New Drug Application

Drug Label Information

Updated July 23, 2014

If you are a consumer or patient please visit this version.

  • Indications and Usage

    Active ingredient (in each tablet)

    Naproxen sodium 220 mg

    (naproxen 200 mg) (NSAID)*

    *nonsteroidal anti-inflammatory drug

    Purpose

    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

    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

    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, or kidney disease
    •you are taking a diuretic
    •you have problems or serious side effects from taking pain relievers or fever reducers
    •you have asthma

    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
    •the risk of heart attack or stroke may increase if you use more than directed or for longer than directed

    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
    •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. (1-800-222-1222)

  • Dosage

    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

    Other information

    •each tablet contains: sodium 21 mg
    •store at 20-25°C (68-77°F). Avoid high humidity and excessive heat above 40°C (104°F).

    Inactive ingredients

    FD&C blue no. 2 aluminum lake, hypromellose, magnesium stearate, microcrystalline cellulose, polyethylene glycol, povidone, talc, titanium dioxide

  • Label

    NDC: 51655-624-24

    MFG: 45802-490-78

    Naproxen Sodium 220 MG

    24 Tablets

    OTC

    Lot#

    Exp. Date:

    Each tablet contains naproxen sodium....220 mg

    Sodium....21 mg

    Dosage: See prescribing information.

    Store at 68 to 77 degrees F

    Store in a tight, light-resistant container. Protect from moisture.

    Keep out of the reach of children.

    Distributed by: Perrigo, Allergan, MI 49010

    Lot#

    Repackaged by Northwind Pharmaceuticals, Indianapolis, IN 46256

    Naproxen Sodium 220 mg 51655-624

  • INGREDIENTS AND APPEARANCE
    NAPROXEN SODIUM 
    naproxen sodium tablet
    Product Information
    Product TypeHUMAN PRESCRIPTION DRUGItem Code (Source)NDC:51655-624(NDC:45802-490)
    Route of AdministrationORAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    NAPROXEN SODIUM (UNII: 9TN87S3A3C) (NAPROXEN - UNII:57Y76R9ATQ) NAPROXEN220 mg
    Product Characteristics
    ColorblueScoreno score
    ShapeROUNDSize10mm
    FlavorImprint Code L490
    Contains    
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:51655-624-2424 in 1 BOTTLE, DISPENSING
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    ANDAANDA07466107/14/2014
    Labeler - Northwind Pharmaceuticals, LLC (036986393)
    Registrant - Northwind Pharmaceuticals, LLC (036986393)
    Establishment
    NameAddressID/FEIBusiness Operations
    Northwind Pharmaceuticals, LLC036986393repack(51655-624)