Is MOMETASONE FUROATE + OLOPATADINE HYDROCHLORIDE registered in Uganda?

MOMETASONE FUROATE + OLOPATADINE HYDROCHLORIDE is recorded with registration status “Registered” in Uganda, registration number NDA/MAL/HDP/10631, based on NDA data.

Who manufactures MOMETASONE FUROATE + OLOPATADINE HYDROCHLORIDE?

MOMETASONE FUROATE + OLOPATADINE HYDROCHLORIDE is manufactured by Glenmark Pharmaceutical Limited Village: Kishnpura, Baddi.

Registered Uganda · NDA

MOMETASONE FUROATE + OLOPATADINE HYDROCHLORIDE

NDA/MAL/HDP/10631 NASAL SYSTEMIC UNIT DOSE AEROSOLS 25 µG + 665 µG

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Registration & product details

Registration no.

NDA/MAL/HDP/10631

Registration date

15/02/2023

Expiry date

Status

Registered

Active ingredient

Dosage form

NASAL SYSTEMIC UNIT DOSE AEROSOLS

Strength

25 µG + 665 µG

Pack size

1*1*240METERED DOSE BOTTLE, 1*1*120METERED DOSE BOTTLE, 1*1*56 METERED DOSE BOTTLE

Therapeutic class

Manufacturer / MAH

Glenmark Pharmaceutical Limited Village: Kishnpura, Baddi

Applicant / LTR

GLENMARK PHARMACEUTICALS LIMITED

Country of origin

INDIA

Manufacturer location

XQH6+46M, Glenmark Rd, Baddi, Himachal Pradesh 174101, India

Source: National Drug Authority · fetched 2026-04-21 17:37:05 · 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.