Registered Uganda · NDA

SERTRALINE HYDROCHLORIDE

NDA/MAL/HDP/0049 ORAL SOLID ORDINARY FILM-COATED TABLETS 100 MG

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Registration & product details

Registration no.
NDA/MAL/HDP/0049
Registration date
01/07/2008
Expiry date
-
Status
Registered
Active ingredient
-
Strength
100 MG
Pack size
I. 1*2*14TABLET BLISTER
Therapeutic class
-
Manufacturer / MAH
Aurobindo Pharma Limited
Applicant / LTR
AUROBINDO PHARMA LIMITED
Country of origin
INDIA
Manufacturer location
Sy. No. 313 Hyderabad, Dr.Reddy's Enclave, Bachupally, Miyapur, Telangana 500118, India

Source: National Drug Authority · fetched 2026-04-21 17:37:05 · updated 2026-09-12 04:00:19

Disclaimer: This information is sourced from National Drug Authority (Uganda). Always consult a qualified healthcare professional before using any medication.