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Mydekla 60 Tablet_

NAFDAC Reg. No. B4-9861 · Drug

Registered with NAFDAC. Registration activeAs of 28 October 2026 · synced automatically from official sources.
Product
Mydekla 60 Tablet_
NAFDAC number
B4-9861
Active ingredient
Daclatasvir (Daclatasvir Dihydrochloride)
Strength
60 mg
Form
Tablet
Pack size
1 x 28's (in HDPE bottle)
Manufacturer
Not listed
Applicant (holder)
Healthline Limited
Approved
27 Aug 2025
Status
Active View on NAFDAC ↗
Registration valid to
26 Aug 2030
WHO alerts
None found
Community reports
None
Times checked
0

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_

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

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

How to take it and how often
  • ?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. …

Possible side effects

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.

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 2025-12-01.

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.

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

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 28 October 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.