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Jopamol-F Tablet

NAFDAC Reg. No. A4-6560 · Drug

Registered with NAFDAC. Registration activeAs of 27 October 2026 · synced automatically from official sources.
Product
Jopamol-F Tablet
NAFDAC number
A4-6560
Active ingredient
Salbutamol (Salbutamol Sulfate); Theophylline
Strength
2 mg; 100 mg
Form
Tablet
Pack size
10 x 10's (in polypropylene tubes)
Manufacturer
Not listed
Applicant (holder)
Yellow Pharmaceutical Company Limited
Approved
6 Jul 2023
Status
Active View on NAFDAC ↗
Registration valid to
5 Jul 2028
WHO alerts
None found
Community reports
None
Times checked
0

What we found

  • Jopamol-F Tablet is on the NAFDAC register with an active registration (A4-6560). 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 Jopamol-F Tablet is used for

From the official U.S. FDA label for salbutamol (salbutamol sulfate), the active ingredient registered with NAFDAC.

What it is used for

Albuterol tablets, USP are indicated for the relief of bronchospasm in adults and children 6 years of age and older with reversible obstructive airway disease.

Possible side effects

The adverse reactions to albuterol are similar in nature to those of other sympathomimetic agents. Albuterol Tablets Adverse Experience Incidence (% of patients) in Adults and Children 6 Years of Age and Older Adverse Event Percent Incidence Central nervous system Nervousness 20 Tremor 20 Headache 7 Dizziness 2 Weakness 2 Sleeplessness 2 Irritability < 1 Drowsiness < 1 Restlessness < 1 Cardiovascular Palpitations 5 Tachycardia 5 Flushing < 1 Chest discomfort < 1 Musculoskeletal Muscle cramps 3 Gastrointestinal Nausea 2 Genitourinary Difficulty in micturition < 1 Albuterol Extended-release Tablets Incidence of Adverse Reactions (% of Patients) in a 1-week Clinical Trials* Adverse Event Albute …

Do not use if

Albuterol tablets are contraindicated in patients with a history of hypersensitivity to albuterol, or any of their components.

Warnings

Paradoxical Bronchospasm Albuterol tablets can produce paradoxical bronchospasm, which may be life threatening. If paradoxical bronchospasm occurs, albuterol tablets should be discontinued immediately and alternative therapy instituted. Deterioration of Asthma Asthma may deteriorate acutely over a period of hours, or chronically over several days or longer. If the patient needs more doses of albuterol tablets than usual, this may be a marker of destabilization of asthma and requires re-evaluation of the patient and the treatment regimen, giving special consideration to the possible need for anti-inflammatory treatment, e.g., corticosteroids. …

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

Check your pack of Jopamol-F 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 Jopamol-F Tablet

What is in Jopamol-F Tablet?

Jopamol-F Tablet contains Salbutamol (Salbutamol Sulfate); Theophylline (2 mg; 100 mg), as tablet, according to its NAFDAC registration record.

Is Jopamol-F Tablet registered with NAFDAC?

Yes. Jopamol-F Tablet is listed on the NAFDAC register under registration number A4-6560, and its registration is active as of 27 October 2026.

Has Jopamol-F Tablet been flagged as fake or recalled?

No WHO falsified or substandard medical product alert currently matches Jopamol-F Tablet in our automatically synced alert list.

How can I check that my pack of Jopamol-F Tablet is genuine?

Run a free authenticity scan with the NAFDAC number A4-6560, 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 Jopamol-F Tablet used for?

Albuterol tablets, USP are indicated for the relief of bronchospasm in adults and children 6 years of age and older with reversible obstructive airway disease. (Summarised from the official U.S. FDA label for salbutamol (salbutamol sulfate). Always follow your doctor or pharmacist.)

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