Is LINAGLIPTIN + METFORMIN HYDROCHLORIDE registered in Uganda?

LINAGLIPTIN + METFORMIN HYDROCHLORIDE is recorded with registration status “Registered” in Uganda, registration number NDA/MAL/HDP/12030, based on NDA data.

Registered Uganda · NDA

LINAGLIPTIN + METFORMIN HYDROCHLORIDE

Q: Who manufactures LINAGLIPTIN + METFORMIN HYDROCHLORIDE?

LINAGLIPTIN + METFORMIN HYDROCHLORIDE is manufactured by Alidac Healthcare Limited Lot No. B19, Zone A, Thilawa Special Economic Zone, Thanlyin Township, Yangon, Myanmar Myanmar.

NDA/MAL/HDP/12030 ORAL SOLID ORDINARY FILM-COATED TABLETS 2.5 MG + 1000 MG

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Registration & product details

Registration no.

NDA/MAL/HDP/12030

Registration date

27/06/2025

Expiry date

Status

Registered

Active ingredient

Dosage form

ORAL SOLID ORDINARY FILM-COATED TABLETS

Strength

2.5 MG + 1000 MG

Pack size

I. 1*3*10TABLET BLISTER

Therapeutic class

Manufacturer / MAH

Alidac Healthcare Limited Lot No. B19, Zone A, Thilawa Special Economic Zone, Thanlyin Township, Yangon, Myanmar Myanmar

Applicant / LTR

CADILA HEALTHCARE LIMITED

Country of origin

MYANMAR

Manufacturer location

B19 , Thilawa Economic Zone A, Thanlyin, Yangon, Myanmar (Burma)

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.