Is LEVOCETIRIZINE DIHYDROCHLORIDE + MONTELUKAST SODIUM registered in Uganda?

LEVOCETIRIZINE DIHYDROCHLORIDE + MONTELUKAST SODIUM is recorded with registration status “Registered” in Uganda, registration number NDA/MAL/HDP/11434, based on NDA data.

Who manufactures LEVOCETIRIZINE DIHYDROCHLORIDE + MONTELUKAST SODIUM?

LEVOCETIRIZINE DIHYDROCHLORIDE + MONTELUKAST SODIUM is manufactured by Cachet Pharmaceutical Pvt Ltd., Village-thana.

Registered Uganda · NDA

LEVOCETIRIZINE DIHYDROCHLORIDE + MONTELUKAST SODIUM

NDA/MAL/HDP/11434 ORAL LIQUID ORDINARY SYRUPS (2.5 MG + 4 MG )/5 ML

Ask about this medicine

Answers come only from this medicine's registration record, BNF monograph and interaction data - not medical advice.

Medicine sourcing is available in Kenya only. We don't sell or dispense medicines - licensed pharmacies do.

Sourcing - Kenya only

Registration & product details

Registration no.

NDA/MAL/HDP/11434

Registration date

01/06/2024

Expiry date

Status

Registered

Active ingredient

Dosage form

ORAL LIQUID ORDINARY SYRUPS

Strength

(2.5 MG + 4 MG )/5 ML

Pack size

1.0X1.0X60.0 ML BOTTLE

Therapeutic class

Manufacturer / MAH

Cachet Pharmaceutical Pvt Ltd., Village-thana

Applicant / LTR

CACHET PHARMACEUTICALS PRIVATE LIMITED

Country of origin

INDIA

Manufacturer location

XQ7J+2XV, Baddi, Himachal Pradesh 173205, India

Source: National Drug Authority · fetched 2026-06-19 02:11:44 · updated 2026-09-12 04:00:20

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