Verifying…
Home / Drug A–Z / Maxpen-V Tablets

Maxpen-V Tablets

NAFDAC Reg. No. 04-7087 · Drug

Registered with NAFDAC. Registration activeAs of 28 October 2026 · synced automatically from official sources.
Product
Maxpen-V Tablets
NAFDAC number
04-7087
Active ingredient
Phenoxymethylpenicillin (Phenoxymethylpenicillin Potassium)
Strength
500,000 IU
Form
Tablet
Pack size
12 x 10's (in plastic tubes)
Manufacturer
Not listed
Applicant (holder)
Nkoyo Chemists Ltd
Approved
29 Mar 2021
Status
Inactive View on NAFDAC ↗
Registration valid to
28 Mar 2026
WHO alerts
None found
Community reports
None
Times checked
0

What we found

  • Maxpen-V Tablets is on the NAFDAC register with an active registration (04-7087). 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.

How to use Maxpen-V Tablets

What the official label says. If a doctor prescribed it, follow the prescription. Your pack's leaflet comes first if it is different.

Who it is for

To reduce the development of drug-resistant bacteria and maintain the effectiveness of penicillin V potassium and other antibacterial drugs, penicillin V potassium should be used only to treat or prevent infections that are proven or strongly suspected to be caused by susceptible bacteria. When culture and susceptibility information are available, they should be considered in selecting or modifying antibacterial therapy. In the absence of such data, local epidemiology and susceptibility patterns may contribute to the empiric selection of therapy. …

How to take it and how often
  • The dosage of Penicillin V should be determined according to the sensitivity of the causative microorganisms and the severity of infection, and adjusted to the clinical response of the patient
  • The usual dosage recommendations for
  • Adults and
  • Children 12 years and over are as follows: Streptococcal Infections Mild to moderately severe - of the upper respiratory tract and including scarlet fever and erysipelas: 125 to 250 mg (200,000 to 400,000 units) every 6 to 8 hours for 10 days
  • Pneumococcal Infections Mild to moderately severe - of the respiratory tract, including otitis media: 250 to 500 mg (400,000 to 800,000 units) every 6 hours until the patient has been afebrile for at least 2 days
  • Staphylococcal Infections Mild infections of skin and soft tissue (culture and sensitive tests should be performed): 250 to 500 mg (400,000 to 800,000 units) every 6 to 8 hours
  • Fusospirochetosis (Vincent’s infection) of the oropharynx
  • Mild to moderately severe infections: 250 to 500 mg (400,000 to 800,000 units) every 6 to 8 hours
  • For the prevention of recurrence following rheumatic fever and/or chorea: 125 mg to 250 mg (200,000 to 400,000 units) twice daily on a continuing basis
  • For prophylaxis against bacterial endocarditis 1 in patients with congenital heart disease or rheumatic or other acquired valvular heart disease when undergoing dental procedures or surgical procedures of the upper respiratory tract: 2 gram of penicillin V (1 gram for
  • Children under 60 lbs.) 1 hour before the procedure, and then, 1 gram (500 mg for
  • Children under 60 lbs.) 6 hours later
While you are taking it
  • Patients should be counseled that antibacterial drugs including penicillin V potassium should only be used to treat bacterial infections
  • They do not treat viral infections (e.g., the common cold)
  • When penicillin V potassium is prescribed to treat a bacterial infection, patients should be told that although it is common to feel better early in the course of therapy, the medication should be taken exactly as directed. …
Talk to a doctor first if

A previous hypersensitivity reaction to any penicillin is a contraindication.

Warnings

SERIOUS AND OCCASIONALLY FATAL HYPERSENSITIVITY (anaphylactic) REACTIONS HAVE BEEN REPORTED IN PATIENTS ON PENICILLIN THERAPY. THESE REACTIONS ARE MORE LIKELY TO OCCUR IN INDIVIDUALS WITH A HISTORY OF PENICILLIN HYPERSENSITIVITY AND/OR A HISTORY OF SENSITIVITY TO MULTIPLE ALLERGENS. THERE HAVE BEEN REPORTS OF INDIVIDUALS WITH A HISTORY OF PENICILLIN HYPERSENSITIVITY WHO HAVE EXPERIENCED SEVERE REACTIONS WHEN TREATED WITH CEPHALOSPORINS. BEFORE INITIATING THERAPY WITH PENICILLIN V POTASSIUM TABLETS, CAREFUL INQUIRY SHOULD BE MADE CONCERNING PREVIOUS HYPERSENSITIVITY REACTIONS TO PENICILLINS, CEPHALOSPORINS, OR OTHER ALLERGENS. …

Possible side effects

Although the incidence of reactions to oral penicillins has been reported with much less frequency than following parenteral therapy, it should be remembered that all degrees of hypersensitivity, including fatal anaphylaxis, have been reported with oral penicillin. The most common reactions to oral penicillin are nausea, vomiting, epigastric distress, diarrhea, and black hairy tongue. The hypersensitivity reactions reported are skin eruptions (maculopapular to exfoliative dermatitis), urticaria and other serum-sickness like reactions, laryngeal edema, and anaphylaxis. Fever and eosinophilia may frequently be the only reaction observed. …

If you miss a dose

Take it when you remember, unless it is nearly time for the next dose. Then skip the missed one. Never take two doses at once to make up for it. Check your leaflet, as some medicines are different.

From the official U.S. FDA label for this active ingredient. Your pack may have a different strength, so always read its leaflet. If a doctor prescribed it, follow the prescription. Ask a pharmacist if you are unsure. Label dated 2025-10-15.

Label for phenoxymethylpenicillin (phenoxymethylpenicillin potassium), the active ingredient registered with NAFDAC.

Check your pack of Maxpen-V Tablets

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

3 free checks left today Official sources: NAFDAC · WHO · U.S. FDA · Health Canada · NLM

About Maxpen-V Tablets

What is in Maxpen-V Tablets?

Maxpen-V Tablets contains Phenoxymethylpenicillin (Phenoxymethylpenicillin Potassium) (500,000 IU), as tablet, according to its NAFDAC registration record.

Is Maxpen-V Tablets registered with NAFDAC?

Yes. Maxpen-V Tablets is listed on the NAFDAC register under registration number 04-7087, and its registration is active as of 28 October 2026.

Has Maxpen-V Tablets been flagged as fake or recalled?

No WHO falsified or substandard medical product alert currently matches Maxpen-V Tablets in our automatically synced alert list.

How can I check that my pack of Maxpen-V Tablets is genuine?

Run a free authenticity scan with the NAFDAC number 04-7087, 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.

How do I take Maxpen-V Tablets?

Follow your prescription or the leaflet in your pack. The official label says: The dosage of Penicillin V should be determined according to the sensitivity of the causative microorganisms and the severity of infection, and adjusted to the clinical response of the patient. The usual dosage recommendations for adults and children 12 years and over are as follows: Streptococcal Infections Mild to moderately severe - of the upper respiratory tract and includi…

What is Maxpen-V Tablets used for?

To reduce the development of drug-resistant bacteria and maintain the effectiveness of penicillin V potassium and other antibacterial drugs, penicillin V potassium should be used only to treat or prevent infections that are proven or strongly suspected to be caused by susceptible bacteria. When culture and susceptibility information are available, they should be considered in selecting or modifyin (Summarised from the official U.S. FDA label for phenoxymethylpenicillin (phenoxymethylpenicillin potassium). Always follow your doctor or pharmacist.)

Patient reviews

–No reviews yet
5★
0
4★
0
3★
0
2★
0
1★
0
Have you used Maxpen-V Tablets? Share your experience to help other patients. Sign in to review

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