Registered Uganda · NDA

CEFOPRAZONE SODIUM + SULBACTUM SODIUM

NDA/MAL/HDP/10376 PARENTERAL ORDINARY DRY VIALS 0.5G + 0.5G

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Registration & product details

Registration no.
NDA/MAL/HDP/10376
Registration date
09/09/2022
Expiry date
-
Status
Registered
Active ingredient
-
Strength
0.5G + 0.5G
Pack size
1.0X1.0X1.0 G VIAL + 1*5ML AMPOULE OF WFI
Therapeutic class
-
Country of origin
PAKISTAN |
Manufacturer location
Sheikhupura-Faisalabad Rd, Bhikhi, Punjab, Chah Chandu, Pakistan

Source: National Drug Authority · fetched 2026-07-11 04:00:21 · 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.