Registered Uganda · NDA

DIPHTHERIA TOXOID+TETANUS TOXOID+PERTUSSIS TOXOID(PT)+FILAMENTOUS HAEMAGGLUTININ(FHA)+PERTACTIN(69KDA OMP)+HBSAG PURIFIED,INACTIVATED POLIO VIRUS TYPE I+INACTIVATED POLIO VIRUS TYPE II+INACTIVATED POLIO VIRUS TYPE III+PURIFIED CAPSULAR POLYSACCHARIDE OF HIB COVALENTLY BOUND TO TETANUS TOXOID(PRP-T)

NDA/MAL/HDP/5124 PARENTERAL ORDINARY COMBINATION PACK VIALS MIN 30 I.U+MIN 40 I.U+25?G+25?G+8?G+10?G,40DU+8DU+32DU+10?G

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Registration & product details

Registration no.
NDA/MAL/HDP/5124
Registration date
01/07/2013
Expiry date
-
Status
Registered
Active ingredient
-
Strength
MIN 30 I.U+MIN 40 I.U+25?G+25?G+8?G+10?G,40DU+8DU+32DU+10?G
Pack size
1.0X1.0 PACK CARTON (DTPA-HBV-IPV IN PREFILLED SYRINGE + 2 NEEDLES+FREEZE DRIED HIB IN A VIAL)
Therapeutic class
-
Applicant / LTR
GSK BIOLOGICALS SA
Country of origin
BELGIUM
Manufacturer location
Rue de l'Institut 89, 1330 Rixensart, Belgium

Source: National Drug Authority · fetched 2026-04-21 17:37:08 · 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.