Is MOXIFLOXACIN HYDROCHLORIDE + DEXAMETHASONE SODIUM PHOSPHATE registered in Uganda?

MOXIFLOXACIN HYDROCHLORIDE + DEXAMETHASONE SODIUM PHOSPHATE is recorded with registration status “Registered” in Uganda, registration number NDA/MAL/HDP/7151, based on NDA data.

Who manufactures MOXIFLOXACIN HYDROCHLORIDE + DEXAMETHASONE SODIUM PHOSPHATE?

MOXIFLOXACIN HYDROCHLORIDE + DEXAMETHASONE SODIUM PHOSPHATE is manufactured by Ciron Drugs & Pharmaceuticals Pvt Ltd, N-118, N-119 Midc Tarapur Boisar Dist Thane 401506 Maharashtra India.

Registered Uganda · NDA

MOXIFLOXACIN HYDROCHLORIDE + DEXAMETHASONE SODIUM PHOSPHATE

NDA/MAL/HDP/7151 OPHTHALMIC DROPS 5MG+1MG/ML

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Registration & product details

Registration no.

NDA/MAL/HDP/7151

Registration date

30/05/2018

Expiry date

Status

Registered

Active ingredient

Dosage form

OPHTHALMIC DROPS

Strength

5MG+1MG/ML

Pack size

1.0X1.0X5.0 ML VIAL

Therapeutic class

Manufacturer / MAH

Ciron Drugs & Pharmaceuticals Pvt Ltd, N-118, N-119 Midc Tarapur Boisar Dist Thane 401506 Maharashtra India

Applicant / LTR

AJANTA PHARMA LIMITED

Country of origin

INDIA

Manufacturer location

118/1, N-118, Navapur Rd, Tarapur M.I.D.C., Pam, Maharashtra 401506, India

Source: National Drug Authority · fetched 2026-04-21 17:37:09 · updated 2026-09-12 04:00:21

Disclaimer: This information is sourced from National Drug Authority (Uganda). Always consult a qualified healthcare professional before using any medication.