Registered Uganda · NDA

CEFOTAXIME

NDA/MAL/HDP/6685 PARENTERAL ORDINARY DRY VIALS 1 G

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Registration & product details

Registration no.
NDA/MAL/HDP/6685
Registration date
01/07/2014
Expiry date
-
Status
Registered
Active ingredient
-
Dosage form
PARENTERAL ORDINARY DRY VIALS
Strength
1 G
Pack size
1.0X1.0 G VIAL
Therapeutic class
-
Manufacturer / MAH
Neon Laboratories Ltd
Applicant / LTR
NEON LABARATORIES LTD.
Country of origin
INDIA
Manufacturer location
Palghar Taluka Industrial Co Operative Estate, Palghar, Maharashtra 401404, India

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.