Is SODIUM CHLORIDE INTRAVENOUS INFUSION (NS) registered in Rwanda?

SODIUM CHLORIDE INTRAVENOUS INFUSION (NS) is recorded with registration status “Registered” in Rwanda, registration number Rwanda FDA-HMP-MA-0531, based on Rwanda FDA data.

Who manufactures SODIUM CHLORIDE INTRAVENOUS INFUSION (NS)?

SODIUM CHLORIDE INTRAVENOUS INFUSION (NS) is manufactured by Abacus Parenteral Drugs.

What is the active ingredient in SODIUM CHLORIDE INTRAVENOUS INFUSION (NS)?

SODIUM CHLORIDE INTRAVENOUS INFUSION (NS) contains Sodium Chloride 0.9% w/v, dosage form Solution for infusion.

Registered Rwanda · Rwanda FDA

SODIUM CHLORIDE INTRAVENOUS INFUSION (NS)

Sodium Chloride 0.9% w/v

Rwanda FDA-HMP-MA-0531 Solution for infusion 0.9% w/v

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Registration & product details

Registration no.

Rwanda FDA-HMP-MA-0531

Registration date

05/10/2023

Expiry date

04/10/2028

Status

Registered

Active ingredient

Sodium Chloride 0.9% w/v

Dosage form

Solution for infusion

Strength

0.9% w/v

Pack size

500 ml & 250 ml Bottles

Therapeutic class

Manufacturer / MAH

Abacus Parenteral Drugs

Applicant / LTR

ABACUS PARENTERAL DRUGS LTD (APDL)

Country of origin

UGANDA

Manufacturer location

Jinja Kampala Road, Mukono, Uganda

Source: Rwanda Food and Drugs Authority · fetched 2026-03-11 22:07:29 · updated 2026-09-21 02:30:20

Disclaimer: This information is sourced from Rwanda Food and Drugs Authority (Rwanda). Always consult a qualified healthcare professional before using any medication.