Registered Uganda · NDA

SODIUM VALPROATE

NDA/MAL/HDP/11955 ORAL LIQUID ORDINARY LIQUIDS 200.0 MG/5ML

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Registration & product details

Registration no.
NDA/MAL/HDP/11955
Registration date
27/06/2025
Expiry date
-
Status
Registered
Active ingredient
-
Dosage form
ORAL LIQUID ORDINARY LIQUIDS
Strength
200.0 MG/5ML
Pack size
I. 1.0*1.0*100.0ML BOTTLE
Therapeutic class
-
Manufacturer / MAH
Akums Drugs & Pharmaceuticals Limited €“ Plant Ii Plot No.:
Applicant / LTR
UNOSOURCE PHARMA LTD
Country of origin
INDIA
Manufacturer location
Plot no 19,20,21, Sector-6A, IIE, SIDCUL, Ranipur, Integrated Industrial Estate, Sector 8A, BHEL Township, Haridwar, Uttarakhand 249403, 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.