To find out about a drug, just type the name or DIN (drug identification number) into the search box or try our alphabetical listing below.
| 02044633 | NU-KETOPROFEN 50MG CAPSULE |
| 02044641 | NU-KETOPROFEN-E 100MG ENTERIC-COATED TABLET |
| 02044781 | NU-KETOPROFEN-E 50MG ENTERIC-COATED TABLET |
| 02200910 | NU-KETOPROFEN-SR 200MG |
Ketoprofen belongs to the class of medications known as nonsteroidal anti-inflammatory drugs (NSAIDs). It reduces swelling, inflammation, and pain and is used for the symptomatic treatment of rheumatoid arthritis, osteoarthritis, and ankylosing spondylitis. Ketoprofen also can be used for the treatment of pain associated with menstrual cramps and for the relief of dental pain, and pain after giving birth, mild to moderate pain associated with sprains and strains.
Your doctor may have suggested this medication for conditions other than the ones listed in these drug information articles. If you have not discussed this with your doctor or are not sure why you are taking this medication, speak to your doctor. Do not stop taking this medication without consulting your doctor.
Do not give this medication to anyone else, even if they have the same symptoms as you do. It can be harmful for people to take this medication if their doctor has not prescribed it.
The recommended adult dose for rheumatoid arthritis and osteoarthritis is 150 mg to 200 mg daily. If given as a short-acting tablet, the dose should be divided into three or four equal doses throughout the day.
For treatment of menstrual cramps and mild-to-moderate pain, the recommended adult dose is 50 mg three or four times daily.
The enteric-coated tablets or sustained-release tablets should be taken one or two hours before meals or at least two hours after meals. Ketoprofen short-acting capsules should be taken immediately after a meal or with food to reduce stomach upset. You should not lie down for about 15 to 30 minutes after taking the medication. If stomach upset occurs and does not go away, contact your doctor. Ketoprofen tablets and capsules should always be swallowed whole.
Rectal suppositories provide an alternative form of the medication. One suppository can be used in the morning and evening (or at bedtime) with appropriate use of ketoprofen tablets throughout the day as required. Ketoprofen suppositories should only be used rectally.
The total daily dose of ketoprofen should not exceed 300 mg (includes any combination of tablets and suppositories).
Many things can affect the dose of medication that a person needs, such as body weight, other medical conditions, and other medications. If your doctor has recommended a dose different from the ones given here, do not change the way that you are taking the medication without consulting your doctor.
It is important that this medication be taken exactly as prescribed by your doctor. If you miss a dose, take it as soon as possible and continue with your regular schedule. If it is almost time for your next dose, skip the missed dose and continue with your regular dosing schedule. Do not take a double dose to make up for a missed one.
Do not dispose of medications in wastewater (e.g. down the sink or in the toilet) or in household garbage. Ask your pharmacist how to dispose of medications that are no longer needed or have expired.

Nu®-Ketoprofen is available as a capsule, and as a tablet in an enteric-coated (E), and sustained-release (SR) form.
Nu®-Keto capsules are available in a strength of 50 mg.
50 mg: Type: capsule. Appearance: dark-green and ivory, hard gelatin casing. Markings: printed "NU 50". Active ingredient: 50 mg of ketoprofen. Nonmedicinal ingredients: colloidal silicon dioxide, croscarmellose sodium, D&C Yellow No. 10, FD&C Green No. 3, FD&C Yellow No. 6, gelatin, lactose, magnesium stearate, sodium lauryl sulfate, and titanium dioxide. The capsules do not contain gluten or tartrazine.
Nu®-Ketoprofen-E is available as a tablet in strengths of 50 mg and 100 mg.
50 mg: Type: tablet. Appearance: round, yellow, enteric-coated. Markings: marked "50" on one side. Active ingredient: 50 mg of ketoprofen. Nonmedicinal ingredients: cellulose acetate phthalate, colloidal silicon dioxide, croscarmellose sodium, D&C Yellow No. 10, dextrates, diethyl phthalate, hydroxypropyl methylcellulose, magnesium stearate, methylcellulose, polyethylene glycol, strong ammonia solution, sunset yellow lake (FD&C Yellow No. 6), and titanium dioxide. The enteric-coated tablets do not contain gluten, tartrazine, or lactose.
100 mg: Type: tablet. Appearance: round, yellow, enteric-coated. Markings: marked "NU" and "100" on one side. Active ingredient: 100 mg of ketoprofen. Nonmedicinal ingredients: cellulose acetate phthalate, colloidal silicon dioxide, croscarmellose sodium, D&C Yellow No. 10, dextrates, diethyl phthalate, hydroxypropyl methylcellulose, magnesium stearate, methylcellulose, polyethylene glycol, strong ammonia solution, sunset yellow lake (FD&C Yellow No. 6), and titanium dioxide. The enteric-coated tablets do not contain gluten, tartrazine, or lactose.
Nu®-Ketoprofen-SR is available as a tablet in a strength of 200 mg.
200 mg: Type: sustained-release tablet. Appearance: round, white, enteric-coated. Markings: marked with "NU" on one side and "200" on the other. Active ingredient: 200 mg of ketoprofen. Nonmedicinal ingredients: colloidal silicon dioxide, dextrates, hydroxypropyl cellulose, hydroxypropyl methylcellulose, magnesium stearate, methanol, polyethylene glycol, polyvinyl acetate phthalate, stearic acid, titanium dioxide, and triethyl citrate. The sustained-release tablets do not contain gluten or tartrazine.
This medication should not be taken by anyone who:
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