Registered Uganda · NDA

RECOMBINANT HUMAN ERYTHROPOIETIN

NDA/MAL/HDP/11882 PARENTERAL ORDINARY DRY VIALS 4000 IU/ML

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Registration & product details

Registration no.
NDA/MAL/HDP/11882
Registration date
06/05/2025
Expiry date
-
Status
Registered
Active ingredient
-
Dosage form
PARENTERAL ORDINARY DRY VIALS
Strength
4000 IU/ML
Pack size
I. 1*1*8000I.U VIAL + 1*2ML AMPOULE WATER FOR INJECTION + 1*3ML SYRINGE FOR INJECTION + 1*2 NEEDLES FOR INJECTION
Therapeutic class
-
Manufacturer / MAH
Biosidus S.a
Applicant / LTR
BIOSIDUS S.A
Country of origin
ARGENTINA
Manufacturer location
Av. Los Quilmes 141, B1876 Bernal Oeste, Provincia de Buenos Aires, Argentina

Source: National Drug Authority · fetched 2026-04-21 17:37:05 · 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.