Registered Uganda · NDA

METHYLPREDNISOLONE SODIUM SUCCINATE

NDA/MAL/HDP/0451 PARENTERAL ORDINARY DRY VIALS 500 MG/VIAL

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Registration & product details

Registration no.
NDA/MAL/HDP/0451
Registration date
01/07/2014
Expiry date
-
Status
Registered
Active ingredient
-
Strength
500 MG/VIAL
Pack size
1.0X500.0 MG VIAL + 1*8ML AMPOULE OF WFI*500MG VIAL
Therapeutic class
-
Applicant / LTR
PT SANBE FARMA
Country of origin
INDONESIA
Manufacturer location
Jl. Industri Cimareme I No.8, Cimareme, Kec. Padalarang, Kabupaten Bandung Barat, Jawa Barat 40553, Indonesia

Source: National Drug Authority · fetched 2026-04-21 17:37:05 · updated 2026-09-12 04:00:19

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