Is AMOKXINATE 452MG SUSPENSION registered in Ghana?

AMOKXINATE 452MG SUSPENSION is recorded with registration status “Valid” in Ghana, registration number FDA/SD.243-010106, based on FDA Ghana data.

Who manufactures AMOKXINATE 452MG SUSPENSION?

AMOKXINATE 452MG SUSPENSION is manufactured by North China Pharmaceuticals.

Valid Ghana · FDA Ghana

AMOKXINATE 452MG SUSPENSION

FDA/SD.243-010106

Ask about this medicine

Answers come only from this medicine's registration record, BNF monograph and interaction data - not medical advice.

Medicine sourcing is available in Kenya only. We don't sell or dispense medicines - licensed pharmacies do.

Sourcing - Kenya only

Registration & product details

Registration no.

FDA/SD.243-010106

Registration date

2024-01-19

Expiry date

2027-02-01

Status

Valid

Active ingredient

Dosage form

Strength

Pack size

Therapeutic class

Manufacturer / MAH

North China Pharmaceuticals

Applicant / LTR

PALB PHARMACEUTICALS LIMITED

Country of origin

Manufacturer location

Hong Kong, Chai Wan, 柴灣利眾街40號富誠工業大廈4字樓B3室

Source: Food and Drugs Authority · fetched 2026-04-18 08:33:11 · updated 2026-10-20 04:00:07

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