Is GUAIFENESIN + BROMHEXINE HYDROCHLORIDE + SALBUTAMOL SULFATE registered in Uganda?

GUAIFENESIN + BROMHEXINE HYDROCHLORIDE + SALBUTAMOL SULFATE is recorded with registration status “Registered” in Uganda, registration number NDA/MAL/HDP/6489, based on NDA data.

Who manufactures GUAIFENESIN + BROMHEXINE HYDROCHLORIDE + SALBUTAMOL SULFATE?

GUAIFENESIN + BROMHEXINE HYDROCHLORIDE + SALBUTAMOL SULFATE is manufactured by Glenmark Pharmaceutical Limited Village: Kishnpura, Baddi.

Registered Uganda · NDA

GUAIFENESIN + BROMHEXINE HYDROCHLORIDE + SALBUTAMOL SULFATE

NDA/MAL/HDP/6489 ORAL LIQUID ORDINARY SYRUPS 100 MG/10ML + 4 MG/10ML + 2 MG/10ML

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Registration & product details

Registration no.

NDA/MAL/HDP/6489

Registration date

01/07/2017

Expiry date

Status

Registered

Active ingredient

Dosage form

ORAL LIQUID ORDINARY SYRUPS

Strength

100 MG/10ML + 4 MG/10ML + 2 MG/10ML

Pack size

I. 1*100ML 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 17:37:08 · 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.