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P-Alaxin 20/160 Dispersible Tablet_

NAFDAC Reg. No. A4-100926 · Drug

Registered with NAFDAC. Registration activeAs of 27 October 2026 · synced automatically from official sources.
Product
P-Alaxin 20/160 Dispersible Tablet_
NAFDAC number
A4-100926
Active ingredient
Dihydroartemisinin; Piperaquine Phosphate
Strength
20 mg; 160 mg
Form
Dispersible tablet
Pack size
1 x 3's, 2 x 3's (in Alu Alu Blisters)
Manufacturer
Not listed
Applicant (holder)
Greenlife Pharmaceutical Limited
Approved
31 Jul 2024
Status
Active View on NAFDAC ↗
Registration valid to
30 Jul 2029
WHO alerts
None found
Community reports
None
Times checked
0

What we found

  • P-Alaxin 20/160 Dispersible Tablet_ is on the NAFDAC register with an active registration (A4-100926). A valid number alone does not prove a pack is genuine — counterfeiters copy real numbers, so also check the expiry date, seal and print quality.

Generated automatically from the NAFDAC register, WHO alerts and community data as of today. This is not medical advice. Always follow your doctor or pharmacist.

What P-Alaxin 20/160 Dispersible Tablet_ is used for

From the official U.S. FDA label for P-Alaxin 20/160 Dispersible Tablet_, the active ingredient registered with NAFDAC.

What it is used for

​Uses temporarily relieves minor aches and pains due to: headache toothache backache menstrual cramps muscular aches minor pain of arthritis

Purpose

s Purposes Pain reliever Pain reliever

Possible side effects

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 trouble breathing weakness in one part or side of body slurred speech leg swelling pain gets worse or lasts more than 10 days redness or swelling is present in the painful area any new symptoms appear

Do not use if

​Do not use with any other drug containing acetaminophen (prescription or nonprescription). If you are not sure whether a drug contains acetaminophen, ask a doctor or pharmacist if you have ever had an allergic reaction to acetaminophen or any other pain reliever right before or after heart surgery

Warnings

​Warnings Acetaminophen liver damage warning Acetaminophen liver damage warning: This product contains acetaminophen. Severe liver damage may occur if you take: with other drugs containing acetaminophen more than 6 caplets in 24 hours, which is the maximum daily amount for this product 3 or more alcoholic drinks every day while using this product Acetaminophen allergy alert Acetaminophen allergy alert: may cause severe skin reactions. Symptoms may include: skin reddening blisters rash If skin reaction occurs, stop use and seek medical help right away. NSAID allergy alert NSAID allergy alert: ibuprofen may cause a severe allergic reaction, especially in people allergic to aspirin. …

Pregnancy & breastfeeding

If pregnant or breast-feeding If pregnant or breast-feeding, ask a health professional before use. It is especially important not to use ibuprofen at 20 weeks or later in pregnancy unless definitely directed to do so by a doctor because it may cause problems in the unborn child or complications during delivery.

General information only, not dosing advice. Always follow the leaflet in your pack and your doctor or pharmacist.

Check your pack of P-Alaxin 20/160 Dispersible Tablet_

Add the expiry date on your pack for a full Trust Score.

3 free checks left today Official sources: NAFDAC Green Book & recalls · WHO · U.S. FDA · NLM RxNorm

About P-Alaxin 20/160 Dispersible Tablet_

What is in P-Alaxin 20/160 Dispersible Tablet_?

P-Alaxin 20/160 Dispersible Tablet_ contains Dihydroartemisinin; Piperaquine Phosphate (20 mg; 160 mg), as dispersible tablet, according to its NAFDAC registration record.

Is P-Alaxin 20/160 Dispersible Tablet_ registered with NAFDAC?

Yes. P-Alaxin 20/160 Dispersible Tablet_ is listed on the NAFDAC register under registration number A4-100926, and its registration is active as of 27 October 2026.

Has P-Alaxin 20/160 Dispersible Tablet_ been flagged as fake or recalled?

No WHO falsified or substandard medical product alert currently matches P-Alaxin 20/160 Dispersible Tablet_ in our automatically synced alert list.

How can I check that my pack of P-Alaxin 20/160 Dispersible Tablet_ is genuine?

Run a free authenticity scan with the NAFDAC number A4-100926, your pack's expiry date and batch number to get a Trust Score, compare the pack with the NAFDAC record (ingredient, strength, form, manufacturer), and buy only from licensed pharmacies.

What is P-Alaxin 20/160 Dispersible Tablet_ used for?

​Uses temporarily relieves minor aches and pains due to: headache toothache backache menstrual cramps muscular aches minor pain of arthritis (Summarised from the official U.S. FDA label for P-Alaxin 20/160 Dispersible Tablet_. Always follow your doctor or pharmacist.)

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Reviews are personal experiences from PillVera users, not medical advice. Report side effects to your doctor and to NAFDAC.