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Mydekla 60 Tablet_

NAFDAC Reg. No. B4-9861 · Drug

Registered with NAFDAC. Registration activeAs of 6 November 2026 · synced automatically from official sources.
Product
Mydekla 60 Tablet_
رقم NAFDAC
B4-9861
المادة الفعالة
Daclatasvir (Daclatasvir Dihydrochloride)
التركيز
60 mg
الشكل
Tablet
حجم العبوة
1 x 28's (in HDPE bottle)
Manufacturer
Not listed
Applicant (holder)
Healthline Limited
Approved
27 Aug 2025
الحالة
Active View on NAFDAC ↗
التسجيل ساري حتى
26 Aug 2030
تنبيهات منظمة الصحة العالمية
None found
Community reports
None
Times checked
0

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

What we found

  • Mydekla 60 Tablet_ is on the NAFDAC register with an active registration (B4-9861). 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 Mydekla 60 Tablet_

ما تقوله النشرة الرسمية. إذا وصفه لك طبيب، فاتبع الوصفة. وإذا اختلفت نشرة عبوتك، فالأولوية لها.

لمن هو

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

كيف يُتناول وكم مرة
  • ?Directions
  • Do not take more than directed
  • Adults and children 12 years and over take 2 caplets every 8 hours while symptoms persist
  • Children under 12 years
  • Ask a doctor
  • Do not take more than 6 caplets in 24 hours, unless directed by a doctor
While you are taking it
  • When using this product
  • Take with food or milk if stomach upset occurs
Talk to a doctor first if
  • Ask a doctor before use if
  • Ask a doctor before use if you have liver disease stomach bleeding warning applies to you you have problems or serious side effects from taking pain relievers you have a history of stomach problems, such as heartburn you have high blood pressure, heart disease, liver cirrhosis, kidney disease, asthma, or had a stroke you are taking a diuretic
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. …

الآثار الجانبية المحتملة

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

Pregnancy and 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.

How to store it

Keep out of reach of children.

إذا نسيت جرعة

تناولها عندما تتذكر، إلا إذا اقترب موعد الجرعة التالية. عندها تخطَّ الجرعة المنسية. لا تتناول جرعتين معًا أبدًا للتعويض. راجع النشرة، فبعض الأدوية مختلفة.

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 2025-12-01.

Label for Mydekla 60 Tablet_, the active ingredient registered with NAFDAC.

Check your pack of Mydekla 60 Tablet_

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

أو التقط صورًا للعبوة
تبقّت 3 عمليات تحقق مجانية اليوم Official sources: U.S. FDA · EMA (EU) · Health Canada · WHO alerts

About Mydekla 60 Tablet_

What is in Mydekla 60 Tablet_?

Mydekla 60 Tablet_ contains Daclatasvir (Daclatasvir Dihydrochloride) (60 mg), as tablet, according to its NAFDAC registration record.

Is Mydekla 60 Tablet_ registered with NAFDAC?

Yes. Mydekla 60 Tablet_ is listed on the NAFDAC register under registration number B4-9861, and its registration is active as of 6 November 2026.

Has Mydekla 60 Tablet_ been flagged as fake or recalled?

No WHO falsified or substandard medical product alert currently matches Mydekla 60 Tablet_ in our automatically synced alert list.

How can I check that my pack of Mydekla 60 Tablet_ is genuine?

Run a free authenticity scan with the NAFDAC number B4-9861, 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 Mydekla 60 Tablet_?

Follow your prescription or the leaflet in your pack. The official label says: ​Directions Do not take more than directed adults and children 12 years and over take 2 caplets every 8 hours while symptoms persist children under 12 years ask a doctor do not take more than 6 caplets in 24 hours, unless directed by a doctor…

What is Mydekla 60 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 Mydekla 60 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.