Ibuprofen description, usages, side effects, indications, overdosage, supplying and lots more!

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Ibuprofen

Polygen Pharmaceuticals LLC
Polygen Pharmaceuticals LLC

Ibuprofen Tablets,  200 mg


FULL PRESCRIBING INFORMATION: CONTENTS*




FULL PRESCRIBING INFORMATION

Active ingredient(s)


Ibuprofen 200 mg (NSAID)*

 * nonsteroidal anti-inflammatory drug


Purpose


Pain reliever/Fever reducer


Use(s)

temporarily relieves minor aches and pain due to:

  • backache
  • headache
  • menstrual cramps
  • minor pain of arthritis
  • muscular aches
  • the common cold
  • toothache
  • temporarily reduces fever

Warnings

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

Symptoms may include: 

  • asthma (wheezing)
  • blisters
  • facial swelling
  • hives
  • rash
  • shock
  • skin reddening

If an allergic reaction occurs, stop use and seek medical help right away.


Stomach bleeding warning:
This product contains an NSAID, which may cause 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 non prescription NSAIDs (aspirin, ibuprofen, naproxen, or others)
  • have 3 or more alcoholic drinks every day while using this product
  • the 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

  • you have problems or serious side effects from taking pain relievers or fever reducers
  • you have a history of stomach problems such as heartburn
  • the stomach bleeding warning applies to you
  • you have high blood pressure, heart disease , kidney disease, liver cirrhosis  
  • you are taking  a diuretic
  • you have asthma

Ask a doctor or pharmacist before use if

  • under a doctor’s care for any serious condition
  • taking aspirin for heart attack or stroke, because ibuprofen may decrease this benefit of aspirin
  • 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 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
  • redness or swelling is present in the painful area
  • any new symptoms occur

Side effects occur. You may report side effects to PolyGen at 1-888-291-7337 and/ or FDA at 1-800-FDA-1088

Pregnancy/Breastfeeding


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 right away. (1-800-222-1222)


Directions


  • do not take more than directed
  • the smallest effective dose should be used
adults and children
12 years and older:
· 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

  •  do not use if seal under cap is broken or missing
  • see end panel for lot number and expiration date


Inactive ingredient


colloidal silicon dioxide, croscarmellose sodium, iron oxide red, magnesium stearate, microcrystalline cellulose, polyethylene glycol, polyvinyl alcohol, pregelatinized starch, talc, titanium dioxide

Storage

  • store between 20-25 °C (68-77 ° F).

Questions


1-888-291-7337


Principal Display Panel


CARTON LABEL PDP

 

NDC: 52605-114-01

 

Compare to the active ingredient in Advil®

 

IBUPROFEN TABLETS, USP 200 mg

PAIN RELIEVER/ FEVER REDUCER (NSAID)

 

100 COATED TABLETS

 

SEE NEW WARNINGS INFORMATION
 


Ibuprofen

BOTTLE LABEL PDP

NDC: 52605-114-01

 

IBUPROFEN TABLETS, USP 200 mg

PAIN RELIEVER/ FEVER REDUCER(NSAID)

 

100 COATED TABLETS

 

SEE NEW WARNINGS INFORMATION



Ibuprofen

CARTON LABEL PDP

 

NDC: 52605-117-01

 

Compare to the active ingredient in Advil®

 

IBUPROFEN TABLETS, USP 200 mg

PAIN RELIEVER/ FEVER REDUCER (NSAID)

 

100 COATED CAPLETS

 

SEE NEW WARNINGS INFORMATION



Ibuprofen





BOTTLE LABEL PDP

NDC: 52605-117-01

 

IBUPROFEN TABLETS, USP 200 mg

PAIN RELIEVER/ FEVER REDUCER(NSAID)

 

100 COATED CAPLETS

 

SEE NEW WARNINGS INFORMATION



Ibuprofen



Ibuprofen

Ibuprofen TABLET, COATED

Product Information

Product Type Human otc drug label Item Code (Source) NDC:52605-114
Route of Administration ORAL DEA Schedule

Active Ingredient/Active Moiety

Ingredient Name Basis of Strength Strength
IBUPROFEN IBUPROFEN 200 mg

Inactive Ingredients

Ingredient Name Strength
CROSCARMELLOSE SODIUM
COLLOIDAL SILICON DIOXIDE
ferric oxide red
MAGNESIUM STEARATE
cellulose, microcrystalline
POLYETHYLENE GLYCOLS
talc
titanium dioxide
STARCH, CORN
POLYVINYL ALCOHOL

Product Characteristics

Color Size Imprint Code Shape
BROWN 10 mm 114 ROUND

Packaging

# Item Code Package Description Marketing Start Date Marketing End Date
1 100 in 1 BOTTLE
2 NDC:52605-114-10 1000 in 1 BOTTLE

Marketing Information

Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
ANDA ANDA091239 2012-06-05


Ibuprofen

Ibuprofen TABLET, COATED

Product Information

Product Type Human otc drug label Item Code (Source) NDC:52605-117
Route of Administration ORAL DEA Schedule

Active Ingredient/Active Moiety

Ingredient Name Basis of Strength Strength
IBUPROFEN IBUPROFEN 200 mg

Inactive Ingredients

Ingredient Name Strength
CROSCARMELLOSE SODIUM
COLLOIDAL SILICON DIOXIDE
ferric oxide red
MAGNESIUM STEARATE
cellulose, microcrystalline
POLYETHYLENE GLYCOLS
talc
titanium dioxide
STARCH, CORN
POLYVINYL ALCOHOL

Product Characteristics

Color Size Imprint Code Shape
BROWN 15 mm 117 CAPSULE

Packaging

# Item Code Package Description Marketing Start Date Marketing End Date
1 100 in 1 BOTTLE
2 NDC:52605-117-01 1 in 1 CARTON

Marketing Information

Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
ANDA ANDA091239 2012-06-05


PLEASE, BE CAREFUL!
Be sure to consult your doctor before taking any medication!
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