Registered Uganda · NDA

TERBINAFINE HYDROCHLORIDE

NDA/MAL/HDP/9320 ORAL SOLID ORDINARY TABLETS 250 MG

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Registration & product details

Registration no.
NDA/MAL/HDP/9320
Registration date
08/09/2020
Expiry date
-
Status
Registered
Active ingredient
-
Strength
250 MG
Pack size
I. 1*2*7TABLET 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 17:37:10 · 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.