International reference: 1 US FDA recall for this ingredient

Failed Dissolution Specifications: Low dissolution results were obtained during stability testing (mefanamic)

US-market enforcement records (OpenFDA), shown for reference - not specific to this product in Tanzania.

Registered Tanzania · TMDA

Meftal 500

Mefanamic Acid 500 mg

TAN 00,213 M01A BLU Tablets -

What it does

Mefanamic acid is a pain reliever that helps reduce inflammation and relieve pain.

Commonly used for: menstrual pain (dysmenorrhea), mild to moderate pain, inflammation

Read more in plain English ↓

Plain-language summary for general understanding - not medical advice. Always follow your pharmacist/doctor.

Ask about this medicine

Answers come only from this medicine's registration record, BNF monograph and interaction data - not medical advice.

Medicine sourcing is available in Kenya only. We don't sell or dispense medicines - licensed pharmacies do.

Sourcing - Kenya only

Registration & product details

Registration no.
TAN 00,213 M01A BLU
Registration date
2024-03-01
Expiry date
2029-02-28
Status
Registered/Compliant
Active ingredient
Mefanamic Acid 500 mg
Dosage form
Tablets
Strength
-
Pack size
-
Therapeutic class
-
Manufacturer / MAH
Blue Cross Laboratories
Country of origin
INDIA
Manufacturer location
Blue Cross Pharma Limited, A12, Ambad Satpur Link Rd, MIDC Ambad, Nashik, Maharashtra 422010, India

Source: Tanzania Medicines and Medical Devices Authority · fetched 2026-03-11 23:44:36 · updated 2026-10-19 03:00:45

Disclaimer: This information is sourced from Tanzania Medicines and Medical Devices Authority (Tanzania). Always consult a qualified healthcare professional before using any medication.

About this medicine

Mefanamic acid is a pain reliever that helps reduce inflammation and relieve pain.

What it treats

  • menstrual pain (dysmenorrhea)
  • mild to moderate pain
  • inflammation

How it works

It works by blocking substances in the body that cause pain and inflammation.

Who it's for

It's for adults and children over the age of 12 who need relief from pain.

AI-assisted summary grounded in BNF data - general information only, not medical advice. Always confirm with your pharmacist or doctor.

Clinical monograph: mefanamic

Mefanamic acid is a non-steroidal anti-inflammatory drug (NSAID) used primarily for the treatment of mild to moderate pain and for the relief of dysmenorrhea. It exhibits analgesic, anti-inflammatory, and antipyretic properties, making it useful in various clinical settings. Mefanamic acid is often used when other NSAIDs are not suitable or when patients are specifically seeking a medication with its profile.

Indications

  • Mild to moderate pain
  • Dysmenorrhea
  • Osteoarthritis
  • Rheumatoid arthritis

Dosage

Children: Refer to the BNF for Children for specific dosing guidelines.

Adults: Refer to the BNF for specific dosing guidelines.

Mechanism of action

Mefanamic acid works by inhibiting the enzyme cyclooxygenase (COX), which is responsible for the conversion of arachidonic acid to prostaglandins. By blocking COX enzymes, mefanamic acid reduces the synthesis of prostaglandins, thereby decreasing inflammation, pain, and fever. It primarily inhibits COX-1 and COX-2, which leads to a reduction in the inflammatory response in tissues.

Pharmacodynamics

The pharmacodynamic effects of mefanamic acid include its ability to decrease pain perception and reduce inflammation. It achieves this through the inhibition of prostaglandin synthesis, which plays a crucial role in mediating pain and inflammatory processes. Mefanamic acid is particularly effective in alleviating menstrual pain due to its pronounced effect on prostaglandin levels related to uterine contractions.

Pharmacokinetics

Mefanamic acid is well absorbed from the gastrointestinal tract, with peak plasma concentrations typically occurring within 2 to 4 hours after oral administration. It has a bioavailability of approximately 90%. The drug is extensively metabolized in the liver, with a half-life ranging from 2 to 4 hours. It is primarily excreted in the urine as metabolites, with less than 1% of the dose being excreted unchanged. The pharmacokinetics can be influenced by factors such as age, liver function, and concurrent medications.

Contra-indications

  • Active peptic ulceration
  • History of gastrointestinal bleeding
  • Severe renal impairment
  • Hypersensitivity to mefanamic acid or any of its components
  • Pregnancy, particularly during the third trimester

Adverse effects

  • Gastrointestinal disturbances (nausea, vomiting, diarrhea)
  • Dizziness
  • Headache
  • Rash or allergic reactions
  • Increased risk of cardiovascular events with long-term use
  • Hepatic dysfunction

Interactions

  • May enhance the effects of anticoagulants such as warfarin
  • May reduce the effect of antihypertensive drugs
  • Concurrent use with other NSAIDs may increase the risk of gastrointestinal side effects
  • Caution with renal excretion drugs due to potential renal impairment

Precautions

  • Use with caution in patients with a history of asthma or allergic reactions
  • Monitor renal function in long-term therapy
  • Evaluate cardiovascular risk factors before initiation
  • Avoid use in dehydration or hypovolemia

Pregnancy

Mefanamic acid is not recommended during pregnancy, especially in the third trimester due to potential effects on the fetal cardiovascular system and possible increase in bleeding risk during delivery.

Breast-feeding

Mefenamic acid is excreted in breast milk; caution is advised when administered to nursing mothers.

Storage

Store at room temperature, away from moisture and heat. Keep out of reach of children.

Formulations

  • Capsules
  • Tablets
  • Oral suspension

AI-synthesized from BNF references - general information only, not a substitute for professional medical advice or the current BNF. Verify doses with a pharmacist.

This drug in other countries

The same active ingredient registered across other registries we cover - including different brands.