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Amdocal 10 Tablet

NAFDAC REG NO: A4-2906 Médicament

Enregistré auprès de NAFDAC. Enregistrement actifAs of 29 October 2026 · synced automatically from official sources.
Produit
Amdocal 10 Tablet
Numéro NAFDAC
A4-2906
Principe actif
Amlodipine (Amlodipine Besilate)
Dosage
10 mg
Forme
Tablet
Conditionnement
3 x 10's (in Alu-Alu blisters)
Fabricant
Non répertorié
Déposant / Titulaire :
Pharmadeal Nigeria Limited
Approuvé
26 Apr 2023
Statut
Actif Vue sur NAFDAC ↗
Enregistrement valable jusqu'au
25 Apr 2028
Alertes OMS
Non trouvé
Community reports
None
Times checked
0

About the medicine: Amlodipine: uses, dosage and brands worldwide

What we found

  • Amdocal 10 Tablet is on the NAFDAC register with an active registration (A4-2906). 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 Amdocal 10 Tablet

Ce que dit la notice officielle. Si un médecin vous l'a prescrit, suivez l'ordonnance. La notice de votre boîte prime si elle est différente.

Pour qui

NORLIQVA is a calcium channel blocker for the treatment of: Hypertension ( 1.1 ) NORLIQVA is indicated for the treatment of hypertension in adults and children 6 years of age and older, to lower blood pressure. Lowering blood pressure reduces the risk of fatal and nonfatal cardiovascular events, primarily strokes and myocardial infarctions. Coronary Artery Disease ( 1.2 ) Chronic Stable Angina Vasospastic Angina (Prinzmetal's or Variant Angina) Angiographically Documented Coronary Artery Disease in patients without heart failure or an ejection fraction

Comment le prendre et à quelle fréquence
  • Adult recommended starting dose: 5 mg orally once daily with a maximum of 10 mg orally once daily
  • Small, fragile, or elderly patients, or patients with hepatic insufficiency may be started on 2.5 mg orally once daily
  • Pediatric starting dose: 2.5 mg to 5 mg orally once daily
  • Adults The usual initial antihypertensive oral dose of NORLIQVA is 5 mg orally once daily, and the maximum dose is 10 mg orally once daily
  • Small, fragile, or elderly patients, or patients with hepatic insufficiency may be started on 2.5 mg orally once daily and this dose may be used when adding NORLIQVA to other antihypertensive therapy [see Clinical Pharmacology ]
  • Adjust dosage according to blood pressure goals
  • In general, wait 7 to 14 days between titration steps
  • Titrate more rapidly, however, if clinically warranted, provided the patient is assessed frequently
  • Angina : The recommended dose for chronic stable or vasospastic angina is 5 mg to 10 mg orally once daily, with the lower dose suggested in the elderly and in patients with hepatic insufficiency
  • Most patients will require 10 mg orally once daily for adequate effect
  • Coronary artery disease : The recommended dose range for patients with coronary artery disease is 5 mg to 10 mg orally once daily
  • In clinical studies, the majority of patients required 10 mg orally once daily [see Clinical Studies ]
  • Children The effective antihypertensive oral dose
  • In pediatric patients ages 6 years of age and older is 2.5 mg to 5 mg orally once daily. …
Strengths it comes in

Oral Solution: 1 mg/mL clear, pale straw-colored solution with a mixed berry flavor. Oral solution: 1 mg/mL ( 3 )

Children
  • Amlodipine (2.5 to 5 mg daily) is effective in lowering blood pressure in patients 6 years of age and older [see Clinical Studies ]
  • Effect of amlodipine on blood pressure in patients less than 6 years of age is not known
  • Hepatic Impairment Patients with hepatic impairment have reduced clearance of amlodipine with a resulting increase of AUC
  • A lower initial dose may be required [see Dosage and Administration ]
Older adults

Clinical studies of amlodipine did not include sufficient numbers of subjects aged 65 and over to determine whether they respond differently from younger subjects. Other reported clinical experience has not identified differences in responses between the elderly and younger patients. …

Talk to a doctor first if
  • NORLIQVA is contraindicated in patients with sensitivity to amlodipine
  • Sensitivity to amlodipine
Medicines it may not mix with

Do not exceed doses greater than 20 mg daily of simvastatin. ( 7.2 ) 7.1 Impact of Other Drugs on Amlodipine CYP3A Inhibitors Co-administration with CYP3A inhibitors (moderate and strong) results in increased systemic exposure to amlodipine and may require dose reduction. Monitor for symptoms of hypotension and edema when amlodipine is co-administered with CYP3A inhibitors to determine the need for dose adjustment [see Clinical Pharmacology (12.3) ] . CYP3A Inducers No information is available on the quantitative effects of CYP3A inducers on amlodipine. Blood pressure should be closely monitored when amlodipine is co-administered with CYP3A inducers. …

Warnings

Symptomatic hypotension is possible, particularly in patients with severe aortic stenosis. However, acute hypotension is unlikely. ( 5.1 ) Worsening angina and acute myocardial infarction can develop after starting or increasing the dose of NORLIQVA, particularly in patients with severe obstructive coronary artery disease. ( 5.2 ) Titrate slowly in patients with severe hepatic impairment. ( 5.3 ) 5.1 Hypotension Symptomatic hypotension is possible, particularly in patients with severe aortic stenosis. Because of the gradual onset of action, acute hypotension is unlikely. …

Effets secondaires possibles

Most common adverse reactions to amlodipine were edema, dizziness, flushing and palpitation which occurred in a dose related manner. Other adverse reactions not clearly dose-related but reported with an incidence >1.0% are fatigue and nausea. ( 6 ) To report SUSPECTED ADVERSE REACTIONS, contact CMP Pharma, Inc. at 1-844-321-1443 or FDA at 1-800-FDA-1088 or www.fda.gov/medwatch . 6.1 Clinical Trials Experience Because clinical trials are conducted under widely varying conditions, adverse reaction rates observed in the clinical trials of a drug cannot be directly compared to rates in the clinical trials of another drug and may not reflect the rates observed in practice. …

Pregnancy and breastfeeding

8.1 Pregnancy Risk Summary: The limited available data based on post-marketing reports with amlodipine use in pregnant women are not sufficient to inform a drug-associated risk for major birth defects and miscarriage. There are risks to the mother and fetus associated with poorly controlled hypertension in pregnancy [see Clinical Considerations] In animal reproduction studies, there was no evidence of adverse developmental effects when pregnant r …

If you take too much

Overdosage might be expected to cause excessive peripheral vasodilation with marked hypotension and possibly a reflex tachycardia. Single oral doses of amlodipine maleate equivalent to 40 mg amlodipine/kg and 100 mg amlodipine/kg in mice and rats, respectively, caused deaths. Single oral amlodipine maleate doses equivalent to 4 or more mg amlodipine/kg or higher in dogs (11 or more times the maximum recommended human dose on a mg/m 2 basis) caused a marked peripheral vasodilation and hypotension. If massive overdose should occur, initiate active cardiac and respiratory monitoring. …

En cas d'oubli

Prenez-le dès que vous y pensez, sauf s'il est presque l'heure de la dose suivante. Dans ce cas, sautez la dose oubliée. Ne prenez jamais deux doses à la fois pour compenser. Vérifiez votre notice, certains médicaments font exception.

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 2026-02-16.

Label for amlodipine (amlodipine besilate), the active ingredient registered with NAFDAC.

Check your pack of Amdocal 10 Tablet

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

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Encore 3 vérifications gratuites aujourd'hui Sources officielles : FDA américaine · EMA (UE) · NAFDAC · alertes OMS

About Amdocal 10 Tablet

What is in Amdocal 10 Tablet?

Amdocal 10 Tablet contains Amlodipine (Amlodipine Besilate) (10 mg), as tablet, according to its NAFDAC registration record.

Is Amdocal 10 Tablet registered with NAFDAC?

Yes. Amdocal 10 Tablet is listed on the NAFDAC register under registration number A4-2906, and its registration is active as of 29 October 2026.

Has Amdocal 10 Tablet been flagged as fake or recalled?

No WHO falsified or substandard medical product alert currently matches Amdocal 10 Tablet in our automatically synced alert list.

How can I check that my pack of Amdocal 10 Tablet is genuine?

Run a free authenticity scan with the NAFDAC number A4-2906, 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 Amdocal 10 Tablet?

Follow your prescription or the leaflet in your pack. The official label says: Adult recommended starting dose: 5 mg orally once daily with a maximum of 10 mg orally once daily. ( 2.1 ) Small, fragile, or elderly patients, or patients with hepatic insufficiency may be started on 2.5 mg orally once daily. ( 2.1 ) Pediatric starting dose: 2.5 mg to 5 mg orally once daily. ( 2.2 ) 2.1 Adults The usual initial antihypertensive oral dose of NORLIQVA is 5 mg or…

What is Amdocal 10 Tablet used for?

NORLIQVA is a calcium channel blocker for the treatment of: Hypertension ( 1.1 ) NORLIQVA is indicated for the treatment of hypertension in adults and children 6 years of age and older, to lower blood pressure. Lowering blood pressure reduces the risk of fatal and nonfatal cardiovascular events, primarily strokes and myocardial infarctions. Coronary Artery Disease ( 1.2 ) Chronic Stable Angina Vas (Summarised from the official U.S. FDA label for amlodipine (amlodipine besilate). Always follow your doctor or pharmacist.)

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