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Duozol Tablets

NAFDAC Reg. Rárá. B4-3093 · Oògùn

Forukọsilẹ pẹlu NAFDAC. Iforukọsilẹ ti nṣiṣe lọwọAs of 29 October 2026 · synced automatically from official sources.
Ọja
Duozol Tablets
Nọmba NAFDAC
B4-3093
Ohun elo ti nṣiṣe lọwọ
Ofloxacin; Ornidazole
Agbara
200 mg; 500 mg
Fọọmu
Tablet
Iwọn iṣakojọpọ
1 x 10's
Olupese
Ko ṣe atokọ
Olubẹwẹ (oluranlowo)
Pharma Ethics Limited
Ti fọwọsi
28 Sep 2021
Ipò
Inactive Wo lórí NAFDAC ↗
Iforukọsilẹ wulo si
27 Sep 2026
Tani o ṣe itaniji
Kosi ikankan ti a rii.
Ijabọ Agbegbe
Kò sí
Àwọn àyẹ̀wò àsìkò
0

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

What we found

  • Duozol Tablets is on the NAFDAC register with an active registration (B4-3093). 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 Duozol Tablets

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

Tani o jẹ fun

Ofloxacin ophthalmic solution is indicated for the treatment of infections caused by susceptible strains of the following bacteria in the conditions listed below:

Bii o ṣe le mu u ati igba melo ni
  • The recommended dosage regimen
  • For the treatment of bacterial conjunctivitis is: Days 1 and 2 Instill one to two drops every two to four hours in the affected eye(s)
  • Days 3 through 7 Instill one to two drops four times daily
  • The recommended dosage regimen
  • For the treatment of bacterial corneal ulcer is: Days 1 and 2 Instill one to two drops into the affected eye every 30 minutes, while awake
  • Awaken at approximately four and six hours after retiring and instill one to two drops
  • Days 3 through 7 to 9 Instill one to two drops hourly, while awake
  • Days 7 to 9 through treatment completion Instill one to two drops, four times daily
Children
  • Safety and effectiveness in infants below the age of one year have not been established
  • Quinolones, including ofloxacin, have been shown to cause arthropathy in immature animals after oral administration; however, topical ocular administration of ofloxacin to immature animals has not shown any arthropathy
  • There is no evidence that the ophthalmic dosage form of ofloxacin has any effect on weight bearing joints
Older adults

No overall differences in safety or effectiveness have been observed between elderly and younger patients.

While you are taking it
  • Avoid contaminating the applicator tip with material from the eye, fingers or other source
  • Systemic quinolones, including ofloxacin, have been associated with hypersensitivity reactions, even following a single dose
  • Discontinue use immediately and contact your physician at the first sign of a rash or allergic reaction
Talk to a doctor first if

Ofloxacin ophthalmic solution is contraindicated in patients with a history of hypersensitivity to ofloxacin, to other quinolones, or to any of the components in this medication (see WARNINGS ).

Medicines it may not mix with

Specific drug interaction studies have not been conducted with ofloxacin ophthalmic solution. However, the systemic administration of some quinolones has been shown to elevate plasma concentrations of theophylline, interfere with the metabolism of caffeine, and enhance the effects of the oral anticoagulant warfarin and its derivatives, and has been associated with transient elevations in serum creatinine in patients receiving cyclosporine concomitantly.

Warnings

NOT FOR INJECTION. Ofloxacin ophthalmic solution should not be injected subconjunctivally, nor should it be introduced directly into the anterior chamber of the eye. There are rare reports of anaphylactic reaction/shock and fatal hypersensitivity reactions in patients receiving systemic quinolones, some following the first dose, including ofloxacin. Some reactions were accompanied by cardiovascular collapse, loss of consciousness, angioedema (including laryngeal, pharyngeal or facial edema), airway obstruction, dyspnea, urticaria, and itching. …

Àbájáde tí ó ṣeéṣe

Ophthalmic use: The most frequently reported drug-related adverse reaction was transient ocular burning or discomfort. Other reported reactions include stinging, redness, itching, chemical conjunctivitis/keratitis, ocular/periocular/facial edema, foreign body sensation, photophobia, blurred vision, tearing, dryness, and eye pain. Rare reports of dizziness and nausea have been received. Refer to WARNINGS for additional adverse reactions. To report SUSPECTED ADVERSE REACTIONS, contact Sentlss at 1--855-473-6847 or FDA at 1-800-FDA-1088 or www.fda.gov/medwatch.

Pregnancy and breastfeeding

Pregnancy: Teratogenic Effects: Ofloxacin has been shown to have an embryocidal effect in rats and in rabbits when given in doses of 810 mg/kg/day (equivalent to 9000 times the maximum recommended daily ophthalmic dose) and 160 mg/kg/day (equivalent to 1800 times the maximum recommended daily ophthalmic dose). These dosages resulted in decreased fetal body weight and increased fetal mortality in rats and rabbits, respectively. …

How to store it

STORAGE: Store at 20° to 25°C (68° to 77°F) [see USP Controlled Room Temperature]. Distributed by: Armas Pharmaceuticals, Inc. Freehold, NJ 07728 USA Manufactured by: Ophtapharm AG, Riethofstrasse 1, Hettlingen, 8442, Switzerland (CHE) for Sentiss Ma …

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 2023-10-23.

Label for ofloxacin and ornidazole, the active ingredient registered with NAFDAC.

Check your pack of Duozol Tablets

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

Or take photos of the pack
3 free checks left today Official sources: U.S. FDA · EMA (EU) · NAFDAC · WHO alerts

About Duozol Tablets

What is in Duozol Tablets?

Duozol Tablets contains Ofloxacin; Ornidazole (200 mg; 500 mg), as tablet, according to its NAFDAC registration record.

Is Duozol Tablets registered with NAFDAC?

Yes. Duozol Tablets is listed on the NAFDAC register under registration number B4-3093, and its registration is active as of 29 October 2026.

Has Duozol Tablets been flagged as fake or recalled?

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

How can I check that my pack of Duozol Tablets is genuine?

Run a free authenticity scan with the NAFDAC number B4-3093, 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 Duozol Tablets?

Follow your prescription or the leaflet in your pack. The official label says: The recommended dosage regimen for the treatment of bacterial conjunctivitis is: Days 1 and 2 Instill one to two drops every two to four hours in the affected eye(s). Days 3 through 7 Instill one to two drops four times daily. The recommended dosage regimen for the treatment of bacterial corneal ulcer is: Days 1 and 2 Instill one to two drops into the affected eye every 30 minu…

What is Duozol Tablets used for?

Ofloxacin ophthalmic solution is indicated for the treatment of infections caused by susceptible strains of the following bacteria in the conditions listed below: (Summarised from the official U.S. FDA label for ofloxacin and ornidazole. 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.