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Ibuprofen by L.N.K. International, Inc.

Medically reviewed on December 16, 2017

Dosage form: tablet, film coated
Ingredients: IBUPROFEN 200mg
Labeler: L.N.K. International, Inc.
NDC Code: 50844-291

Ibuprofen Tablets USP, 200 mg

Active ingredient (in each brown tablet)

Ibuprofen USP, 200 mg (NSAID)*
*nonsteroidal anti-inflammatory drug

Purpose

Pain reliever/fever reducer

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

Warnings

Allergy alert: Ibuprofen may cause a severe allergic reaction, especially in people allergic to aspirin. Symptoms may include:

  • hives
  • facial swelling
  • asthma (wheezing)
  • skin reddening
  • shock
  • 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
  • right before or after heart surgery
  • if you have ever had an allergic reaction to any other pain reliever/fever reducer

Ask a doctor before use if
  • stomach bleeding warning applies to you
  • you have problems or serious side effects from taking pain relievers or fever reducers
  • 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

Ask a doctor or pharmacist before use if you are
  • taking aspirin for heart attack or stroke, because ibuprofen may decrease this benefit of aspirin
  • 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
    • weakness in one part or side of body
    • leg swelling
    • slurred speech
    • trouble breathing
  • pain gets worse or lasts more than 10 days
  • fever gets worse or lasts more than 3 days
  • any new symptoms appear
  • redness or swelling is present in the painful area

If pregnant or breast-feeding,

ask a health professional before use. It is especially important not to use ibuprofen 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 (1-800-222-1222) right away.

Directions
  • do not take more than directed
  • the smallest effective dose should be used
  • adults and children 12 years and over: take 1 tablet every 4 to 6 hours while symptoms persist
    • if pain or fever does not respond to 1 tablet, 2 tablets may be used
    • do not exceed 6 tablets in 24 hours, unless directed by a doctor
  • children under 12 years: ask a doctor

Other information
  • store between 20°-25°C (68°-77°F)
  • avoid excessive heat 40°C (104°F)
  • use by expiration date on package

Inactive ingredients

carnauba wax, colloidal silicon dioxide, corn starch, hypromellose, lactose anhydrous, magnesium stearate, microcrystalline cellulose, polydextrose, polyethylene glycol, red iron oxide, sodium starch glycolate, stearic acid, titanium dioxide

Questions or comments?

Call 1-800-426-9391 8:30 AM-4:00 PM ET, Monday-Friday

Principal Display Panel

Quality
+
Plus

NDC 50844-291-16

†Compare to active ingredient
in Advil® Tablets

IBUPROFEN TABLETS
USP, 200 mg

PAIN RELIEVER/
FEVER REDUCER (NSAID)

1000 Coated Tablets

ACTUAL
SIZE

TAMPER EVIDENT: DO NOT USE IF IMPRINTED SAFETY
SEAL UNDER CAP IS BROKEN OR MISSING

†This product is not manufactured or distributed by Wyeth Consumer
Healthcare, owner of the registered trademark Advil® Tablets.
50844            REV1116B29116

Distributed by
LNK INTERNATIONAL, INC.
60 Arkay Drive, Hauppauge, NY 11788
USA

Quality Plus 44-291

IBUPROFEN 
ibuprofen tablet, film coated
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:50844-291
Route of AdministrationORALDEA Schedule    
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
IBUPROFEN (IBUPROFEN) IBUPROFEN200 mg
Inactive Ingredients
Ingredient NameStrength
CARNAUBA WAX 
STARCH, CORN 
HYPROMELLOSE, UNSPECIFIED 
MAGNESIUM STEARATE 
POLYDEXTROSE 
POLYETHYLENE GLYCOL, UNSPECIFIED 
STEARIC ACID 
TITANIUM DIOXIDE 
MICROCRYSTALLINE CELLULOSE 
ANHYDROUS LACTOSE 
SILICON DIOXIDE 
FERRIC OXIDE RED 
SODIUM STARCH GLYCOLATE TYPE A POTATO 
Product Characteristics
ColorBROWNScoreno score
ShapeROUNDSize10mm
FlavorImprint Code44;291
Contains    
Packaging
#Item CodePackage Description
1NDC:50844-291-021 BOTTLE, PLASTIC in 1 CARTON
112 TABLET, FILM COATED in 1 BOTTLE, PLASTIC
2NDC:50844-291-081 BOTTLE, PLASTIC in 1 CARTON
224 TABLET, FILM COATED in 1 BOTTLE, PLASTIC
3NDC:50844-291-011 BOTTLE, PLASTIC in 1 CARTON
330 TABLET, FILM COATED in 1 BOTTLE, PLASTIC
4NDC:50844-291-101 BOTTLE, PLASTIC in 1 CARTON
440 TABLET, FILM COATED in 1 BOTTLE, PLASTIC
5NDC:50844-291-111 BOTTLE, PLASTIC in 1 CARTON
560 TABLET, FILM COATED in 1 BOTTLE, PLASTIC
6NDC:50844-291-121 BOTTLE, PLASTIC in 1 CARTON
6100 TABLET, FILM COATED in 1 BOTTLE, PLASTIC
7NDC:50844-291-291 BOTTLE, PLASTIC in 1 CARTON
7150 TABLET, FILM COATED in 1 BOTTLE, PLASTIC
8NDC:50844-291-131 BOTTLE, PLASTIC in 1 CARTON
8250 TABLET, FILM COATED in 1 BOTTLE, PLASTIC
9NDC:50844-291-0310 TABLET, FILM COATED in 1 BOTTLE, PLASTIC
10NDC:50844-291-14500 TABLET, FILM COATED in 1 BOTTLE, PLASTIC
11NDC:50844-291-161000 TABLET, FILM COATED in 1 BOTTLE, PLASTIC
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
ANDAANDA07501005/24/1988
Labeler - L.N.K. International, Inc. (038154464)
Establishment
NameAddressID/FEIOperations
LNK International, Inc.038154464PACK(50844-291)
Establishment
NameAddressID/FEIOperations
LNK International, Inc.832867894MANUFACTURE(50844-291)
Establishment
NameAddressID/FEIOperations
LNK International, Inc.832867837PACK(50844-291)
Establishment
NameAddressID/FEIOperations
LNK International, Inc.967626305PACK(50844-291)
Establishment
NameAddressID/FEIOperations
LNK International, Inc.868734088PACK(50844-291)

 
L.N.K. International, Inc.

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Further information

Always consult your healthcare provider to ensure the information displayed on this page applies to your personal circumstances.

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