Registered Uganda · NDA

CEFTRIAXONE SODIUM

NDA/MAL/HDP/9867 PARENTERAL ORDINARY DRY VIALS 1G

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Registration & product details

Registration no.
NDA/MAL/HDP/9867
Registration date
21/12/2021
Expiry date
-
Status
Registered
Active ingredient
-
Strength
1G
Pack size
1.0X1.0 G VIAL,1.0X10.0X1.0 G VIAL
Therapeutic class
-
Manufacturer / MAH
Inject Care Parenterals Pvt Ltd
Applicant / LTR
ASTRA PHARMA UGANDA LTD
Country of origin
CHINA
Manufacturer location
Plot 130, Silvassa Road, GIDC Vapi, Phase 2, GIDC, Vapi, Gujarat 396195, India

Source: National Drug Authority · fetched 2026-04-21 17:37:11 · 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.