Is LEVOSALBUTAMOL SULPHATE + AMBROXOL HYDROCHLORIDE + GUAIFENESIN registered in Uganda?

LEVOSALBUTAMOL SULPHATE + AMBROXOL HYDROCHLORIDE + GUAIFENESIN is recorded with registration status “Registered” in Uganda, registration number NDA/MAL/HDP/6424, based on NDA data.

Who manufactures LEVOSALBUTAMOL SULPHATE + AMBROXOL HYDROCHLORIDE + GUAIFENESIN?

LEVOSALBUTAMOL SULPHATE + AMBROXOL HYDROCHLORIDE + GUAIFENESIN is manufactured by Glenmark Pharmaceuticals Ltd ., Village Kishanpura, Baddi-nalagarh Road, Tehsil Baddi, District Solan Hp 173205.

Registered Uganda · NDA

LEVOSALBUTAMOL SULPHATE + AMBROXOL HYDROCHLORIDE + GUAIFENESIN

NDA/MAL/HDP/6424 ORAL LIQUID ORDINARY LIQUIDS 1 MG + 30 MG + 100 MG

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Registration & product details

Registration no.

NDA/MAL/HDP/6424

Registration date

27/03/2019

Expiry date

Status

Registered

Active ingredient

Dosage form

ORAL LIQUID ORDINARY LIQUIDS

Strength

1 MG + 30 MG + 100 MG

Pack size

1.0X1.0X100.0 ML BOTTLE

Therapeutic class

Manufacturer / MAH

Glenmark Pharmaceuticals Ltd ., Village Kishanpura, Baddi-nalagarh Road, Tehsil Baddi, District Solan Hp 173205

Applicant / LTR

GLENMARK PHARMACEUTICALS LTD

Country of origin

INDIA

Manufacturer location

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

Source: National Drug Authority · fetched 2026-04-21 17:37:08 · 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.