Registered Uganda · NDA

RABEPRAZOLE SODIUM

NDA/MAL/HDP/10877 PARENTERAL ORDINARY DRY VIALS 20 MG/VIAL

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Registration & product details

Registration no.
NDA/MAL/HDP/10877
Registration date
05/09/2023
Expiry date
-
Status
Registered
Active ingredient
-
Strength
20 MG/VIAL
Pack size
1.0X1.0X20.0 MG VIAL + 1*10 ML WATER FOR INJECTION IN LDPE CONTAINER
Therapeutic class
-
Country of origin
INDIA
Manufacturer location
8C7M+M35, Chadasna, Gujarat 384450, 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.