Registered Uganda · NDA

YELLOW FEVER VIRUS 17D-204 STRAIN(LIVE ATTENUATED)

NDA/MAL/HDP/1482 PARENTERAL ORDINARY VIALS NLT 1000 I.U

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Registration & product details

Registration no.
NDA/MAL/HDP/1482
Registration date
01/07/1997
Expiry date
-
Status
Registered
Active ingredient
-
Strength
NLT 1000 I.U
Pack size
1.0X1.0 DOSE VIAL + 0.5ML OF SOLVENT IN PRE-FILLED SYRINGE,1.0X10.0X10.0 DOSE VIAL + 1*10*10 DOSE AMPOULE OF NS
Therapeutic class
-
Manufacturer / MAH
Sanofi Pasteur
Applicant / LTR
SANOFI PASTEUR
Country of origin
FRANCE
Manufacturer location
1541 Av. Marcel Mérieux, 69280 Marcy-l'Étoile, France

Source: National Drug Authority · fetched 2026-04-21 17:37:06 · 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.