Registered Uganda · NDA

GEMCITABINE HYDROCHLORIDE

NDA/MAL/HDP/11861 PARENTERAL ORDINARY DRY VIALS 200 MG/VIAL

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Registration & product details

Registration no.
NDA/MAL/HDP/11861
Registration date
06/05/2025
Expiry date
-
Status
Registered
Active ingredient
-
Strength
200 MG/VIAL
Pack size
I. 1*1*10ML VIAL
Therapeutic class
-
Country of origin
INDIA
Manufacturer location
Plot no B-1, Main road, Wagle Industrial Estate, Thane West, Thane, Maharashtra 400604, 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.