Is SODIUM CHLORIDE INTRAVENOUS INFUSION BP registered in Kenya?

SODIUM CHLORIDE INTRAVENOUS INFUSION BP is recorded with registration status “Registered” in Kenya, registration number CTD4835, based on PPB data.

Who manufactures SODIUM CHLORIDE INTRAVENOUS INFUSION BP?

SODIUM CHLORIDE INTRAVENOUS INFUSION BP is manufactured by Dawa.

What is the active ingredient in SODIUM CHLORIDE INTRAVENOUS INFUSION BP?

SODIUM CHLORIDE INTRAVENOUS INFUSION BP contains SODIUM CHLORIDE BP, dosage form EACH 100 ML CONTAINS: SODIUM CHLORIDE BP 0.9 GM.

Registered Kenya · PPB

SODIUM CHLORIDE INTRAVENOUS INFUSION BP

SODIUM CHLORIDE BP

CTD4835 EACH 100 ML CONTAINS: SODIUM CHLORIDE BP 0.9 GM GENERIC/BIOSIMILARS

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Registration & product details

Registration no.

CTD4835

Registration date

Expiry date

Status

Registered

Active ingredient

SODIUM CHLORIDE BP

Dosage form

EACH 100 ML CONTAINS: SODIUM CHLORIDE BP 0.9 GM

Strength

Pack size

1 X 500 ML LDPE BOTTLE

Therapeutic class

GENERIC/BIOSIMILARS

Manufacturer / MAH

Dawa

Applicant / LTR

MEDISEL KENYA LIMITED

Country of origin

FOREIGN

Manufacturer location

Baba Dogo Rd, Nairobi, Kenya

Source: Pharmacy and Poisons Board · fetched 2026-01-28 20:09:38 · updated 2026-08-03 04:09:55

Disclaimer: This information is sourced from Pharmacy and Poisons Board (Kenya). Always consult a qualified healthcare professional before using any medication.