Registered Uganda · NDA

SODIUM CHLORIDE

NDA/MAL/HDP/11939 PARENTERAL ORDINARY INFUSION VIALS/BOTTLES 0.9 %W/V

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Registration & product details

Registration no.
NDA/MAL/HDP/11939
Registration date
27/06/2025
Expiry date
-
Status
Registered
Active ingredient
-
Dosage form
PARENTERAL ORDINARY INFUSION VIALS/BOTTLES
Strength
0.9 %W/V
Pack size
I. 1.0*500.0ML BOTTLE
Therapeutic class
-
Manufacturer / MAH
Amanta Healthcare Limited Plot No
Applicant / LTR
AMANTA HEALTHCARE LIMITED
Country of origin
INDIA
Manufacturer location
876, NH No. 8, Hariyala, Gujarat 387411, 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.