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Home / Registered in Nigeria / Pendorex Cough Mixture 100 mL_

Pendorex Cough Mixture 100 mL_

NAFDAC Reg. No. A11-100663 · Drug

Registered with NAFDAC. Registration activeAs of 6 November 2026 · synced automatically from official sources.
Product
Pendorex Cough Mixture 100 mL_
NAFDAC number
A11-100663
Active ingredient
Ammonium Chloride; Sodium Citrate; Menthol
Strength
110 mg/5 mL; 40 mg/5 mL; 1.1 mg/5 mL
Form
Syrup
Pack size
1 x 100 mL (in amber PET bottle)
Manufacturer
Not listed
Applicant (holder)
MUCHIS HEALTHCARE LIMITED
Approved
28 Feb 2024
Status
Active View on NAFDAC ↗
Registration valid to
27 Feb 2029
WHO alerts
None found
Community reports
None
Times checked
0

About the medicine: Ammonium chloride: uses, dosage and brands worldwide

What we found

  • Pendorex Cough Mixture 100 mL_ is on the NAFDAC register with an active registration (A11-100663). 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 Pendorex Cough Mixture 100 mL_

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

Low back pain and constipation*

How to take it and how often

Adults and children: At the onset of symptoms, dissolve 5 pellets under the tongue 3 times a day until symptoms are relieved or as directed by a doctor.

Possible side effects

Symptoms persist for more than 3 days or worsen

Pregnancy and breastfeeding

If pregnant or breast-feeding ask a health professional before use

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 2023-10-16.

Label for ammonium chloride, the active ingredient registered with NAFDAC.

Check your pack of Pendorex Cough Mixture 100 mL_

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

Or take photos of the pack
3 free checks left today Official sources: U.S. FDA · EMA (EU) · Health Canada · WHO alerts

About Pendorex Cough Mixture 100 mL_

What is in Pendorex Cough Mixture 100 mL_?

Pendorex Cough Mixture 100 mL_ contains Ammonium Chloride; Sodium Citrate; Menthol (110 mg/5 mL; 40 mg/5 mL; 1.1 mg/5 mL), as syrup, according to its NAFDAC registration record.

Is Pendorex Cough Mixture 100 mL_ registered with NAFDAC?

Yes. Pendorex Cough Mixture 100 mL_ is listed on the NAFDAC register under registration number A11-100663, and its registration is active as of 6 November 2026.

Has Pendorex Cough Mixture 100 mL_ been flagged as fake or recalled?

No WHO falsified or substandard medical product alert currently matches Pendorex Cough Mixture 100 mL_ in our automatically synced alert list.

How can I check that my pack of Pendorex Cough Mixture 100 mL_ is genuine?

Run a free authenticity scan with the NAFDAC number A11-100663, 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 Pendorex Cough Mixture 100 mL_?

Follow your prescription or the leaflet in your pack. The official label says: Adults and children: At the onset of symptoms, dissolve 5 pellets under the tongue 3 times a day until symptoms are relieved or as directed by a doctor.…

What is Pendorex Cough Mixture 100 mL_ used for?

Low back pain and constipation* (Summarised from the official U.S. FDA label for ammonium chloride. 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.