Registered Uganda · NDA

FORTIFIED PROCAINE PENICILLIN SODIUM

NDA/MAL/HDP/1535 PARENTERAL ORDINARY DRY VIALS 4 M.U

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Registration & product details

Registration no.
NDA/MAL/HDP/1535
Registration date
01/07/2011
Expiry date
-
Status
Registered
Active ingredient
-
Dosage form
PARENTERAL ORDINARY DRY VIALS
Strength
4 M.U
Pack size
1.0X50.0X4.0 MU VIAL,1.0X100.0X4.0 MU VIAL,1.0X10.0X4.0 MU VIAL
Therapeutic class
-
Manufacturer / MAH
Reyoung Pharmaceutical Co. Limited
Applicant / LTR
ABACUS (A) PHARMA LTD
Country of origin
CHINA

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.