Registered Uganda · NDA

BENZYLPENICILLIN SODIUM

NDA/MAL/HDP/2796 PARENTERAL ORDINARY DRY VIALS 1,000,000I.U

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Registration & product details

Registration no.
NDA/MAL/HDP/2796
Registration date
01/07/2001
Expiry date
-
Status
Registered
Active ingredient
-
Strength
1,000,000I.U
Pack size
1.0X10.0 VIAL CARTON,1.0X50.0 VIAL CARTON
Therapeutic class
-
Applicant / LTR
ASTRA PHARMA (UK) LTD
Country of origin
CHINA

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