Registered Uganda · NDA

CEFOPRAZONE SODIUM + SULBACTUM SODIUM

NDA/MAL/HDP/10172 PARENTERAL ORDINARY DRY VIALS (1G + 1G)/VIAL

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Registration & product details

Registration no.
NDA/MAL/HDP/10172
Registration date
09/09/2022
Expiry date
-
Status
Registered
Active ingredient
-
Strength
(1G + 1G)/VIAL
Pack size
1.0X1.0X2.0 G VIAL + 10ML WFI CLEAR GLASS AMPOULE
Therapeutic class
-
Country of origin
PAKISTAN |
Manufacturer location
Sheikhupura-Faisalabad Rd, Bhikhi, Punjab, Chah Chandu, Pakistan

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.