Registered Uganda · NDA

METHYLPREDNISOLONE HEMISUCCINATE

NDA/MAL/HDP/5030 PARENTERAL ORDINARY DRY VIALS 125MG/2ML

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Registration & product details

Registration no.
NDA/MAL/HDP/5030
Registration date
01/07/1997
Expiry date
-
Status
Registered
Active ingredient
-
Dosage form
PARENTERAL ORDINARY DRY VIALS
Strength
125MG/2ML
Pack size
1.0X2.0 ML VIAL,1.0X8.0 ML VIAL
Therapeutic class
-
Manufacturer / MAH
Pfizer Global Manufacturing Belgium Nv, Rijksweg 12
Applicant / LTR
PFIZER LAB LTD
Country of origin
BELGIUM
Manufacturer location
Rijksweg 12, 2870 Puurs-Sint-Amands, Belgium

Source: National Drug Authority · fetched 2026-04-21 17:37:07 · updated 2026-09-12 04:00:21

Disclaimer: This information is sourced from National Drug Authority (Uganda). Always consult a qualified healthcare professional before using any medication.