Is ABACAVIR SULFATE + DOLUTEGRAVIR SODIUM + LAMIVUDINE registered in Uganda?

ABACAVIR SULFATE + DOLUTEGRAVIR SODIUM + LAMIVUDINE is recorded with registration status “Registered” in Uganda, registration number NDA/MAL/HDP/11427, based on NDA data.

Who manufactures ABACAVIR SULFATE + DOLUTEGRAVIR SODIUM + LAMIVUDINE?

ABACAVIR SULFATE + DOLUTEGRAVIR SODIUM + LAMIVUDINE is manufactured by Hetero Labs Limited, Sy. No. 439.

Registered Uganda · NDA

ABACAVIR SULFATE + DOLUTEGRAVIR SODIUM + LAMIVUDINE

NDA/MAL/HDP/11427 ORAL SOLID ORDINARY FILM-COATED TABLETS 600MG + 50MG + 300MG

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/11427

Registration date

01/06/2024

Expiry date

Status

Registered

Active ingredient

Dosage form

ORAL SOLID ORDINARY FILM-COATED TABLETS

Strength

600MG + 50MG + 300MG

Pack size

1.0X30.0 TABLET CONTAINER

Therapeutic class

Manufacturer / MAH

Hetero Labs Limited, Sy. No. 439

Applicant / LTR

M/S HETERO LABS LIMITED

Country of origin

INDIA

Manufacturer location

R4FJ+RMP, Gollapalle, Telangana 509302, 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.