Registered Uganda · NDA

HYDROCORTISONE SODIUM SUCCINATE

NDA/MAL/HDP/1678 PARENTERAL ORDINARY DRY VIALS 100MG/VIAL

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Registration & product details

Registration no.
NDA/MAL/HDP/1678
Registration date
01/07/2007
Expiry date
-
Status
Registered
Active ingredient
-
Strength
100MG/VIAL
Pack size
1.0X10.0X100.0 MG VIAL,1.0X50.0X100.0 MG VIAL
Therapeutic class
-
Applicant / LTR
ASTRA PHARMA (U) LIMITED
Country of origin
INDIA
Manufacturer location
FV56+WX8, Bhimpore, Daman, Dadra and Nagar Haveli and Daman and Diu 396210, India

Source: National Drug Authority · fetched 2026-04-21 17:37:06 · 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.