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Duban Injection

NAFDAC Reg. Rárá. B4-3671 · Oògùn

Forukọsilẹ pẹlu NAFDAC. Iforukọsilẹ ti nṣiṣe lọwọAs of 31 October 2026 · synced automatically from official sources.
Ọja
Duban Injection
Nọmba NAFDAC
B4-3671
Ohun elo ti nṣiṣe lọwọ
Chloramphenicol (Chloramphenicol Sodium Succinate)
Agbara
1 g
Fọọmu
Powder for injection
Iwọn iṣakojọpọ
1 x 10 mL vial
Olupese
Ko ṣe atokọ
Olubẹwẹ (oluranlowo)
Maydon Pharmaceuticals Limited
Ti fọwọsi
16 Dec 2021
Ipò
Nṣiṣẹ Wo lórí NAFDAC ↗
Iforukọsilẹ wulo si
15 Dec 2026
Tani o ṣe itaniji
Kosi ikankan ti a rii.
Ijabọ Agbegbe
Kò sí
Àwọn àyẹ̀wò àsìkò
0

Nipa oogun naa: Chloramphenicol: uses, dosage and brands worldwide

What we found

  • Duban Injection is on the NAFDAC register with an active registration (B4-3671). 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 Duban Injection

What the official label says. If a doctor prescribed it, follow the prescription. Your pack's leaflet comes first if it is different.

Serious warning: Serious and fatal blood dyscrasias (aplastic anemia, hypoplastic anemia, thrombocytopenia and granulocytopenia) are known to occur after the administration of chloramphenicol. In addition, there have been reports of aplastic anemia attributed to chloramphenicol which later terminated in leukemia. Blood dyscrasias have occurred after both short-term and prolonged therapy with this drug. …
Children
  • Precaution should be used in therapy of premature and full-term
  • Neonates and infants to avoid “gray syndrome” toxicity
  • Due to immature metabolic processes in the neonate and infant, excessive blood levels may result from administration of the recommended dose
  • The dosage should be adjusted accordingly or, preferable, the blood concentration should be determined at appropriate intervals (see ADVERSE REACTIONS , "Gray Syndrome" )
  • See DOSAGE AND ADMINISTRATION for dosing information in the pediatric population
Older adults

Clinical studies of chloramphenicol sodium succinate 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
  • Chloramphenicol is contraindicated in individuals with a history of previous hypersensitivity and/or toxic reaction to it
  • It must not be used in the treatment of trivial infections or where it is not indicated, as in colds, influenza, infections of the throat; or as a prophylactic agent to prevent bacterial infections
Medicines it may not mix with

Concurrent therapy with other drugs that may cause bone marrow depression should be avoided.

Warnings

PRECAUTIONS: General Repeated courses of chloramphenicol treatment should be avoided if at all possible. Treatment should not be continued longer than required to produce a cure with little or no risk or relapse of the disease. Excessive blood levels may result from administration of the recommended dose to patients with impaired liver or kidney function. The dosage should be adjusted accordingly, or preferably, the blood concentration should be determined at appropriate intervals. The use of this antibiotic, as with other antibiotics, may result in an overgrowth of nonsusceptible organisms, including fungi. …

Àbájáde tí ó ṣeéṣe

Blood Dyscrasias The most serious adverse effect of chloramphenicol is bone marrow depression. Serious and fatal blood dyscrasias (aplastic anemia, hypoplastic anemia, thrombocytopenia, and granulocytopenia) are known to occur after the administration of chloramphenicol. An irreversible type of marrow depression leading to aplastic anemia with a high rate of mortality is characterized by the appearance weeks or months after therapy of bone marrow aplasia or hypoplasia. Peripherally, pancytopenia is most often observed, but in a small number of cases only one or two of the three major cell types (erythrocytes, leukocytes, platelets) may be depressed. …

Pregnancy and breastfeeding

Pregnancy Pregnancy Category C – Animal reproduction studies have not been conducted with chloramphenicol. There are no adequate and well-controlled studies to establish safety of this drug in pregnancy. It is not known whether chloramphenicol can cause fetal harm when administered to a pregnant woman. Orally administered chloramphenicol has been shown to cross the placental barrier. …

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 2024-10-10.

Label for chloramphenicol (chloramphenicol sodium succinate), the active ingredient registered with NAFDAC.

Check your pack of Duban Injection

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

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3 free checks left today Official sources: U.S. FDA · EMA (EU) · NAFDAC · WHO alerts

About Duban Injection

What is in Duban Injection?

Duban Injection contains Chloramphenicol (Chloramphenicol Sodium Succinate) (1 g), as powder for injection, according to its NAFDAC registration record.

Is Duban Injection registered with NAFDAC?

Yes. Duban Injection is listed on the NAFDAC register under registration number B4-3671, and its registration is active as of 31 October 2026.

Has Duban Injection been flagged as fake or recalled?

No WHO falsified or substandard medical product alert currently matches Duban Injection in our automatically synced alert list.

How can I check that my pack of Duban Injection is genuine?

Run a free authenticity scan with the NAFDAC number B4-3671, 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.

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