Search Drugs Database

Detail Information

Last Updated: 18-Sep-2026

Product Name

AMINOLEBAN ORAL POWDER

Registration No.

HK-54177

Certificate Holder

OTSUKA PHARMACEUTICAL (H.K.) LIMITED

Certificate Holder Address

RM 1801, 18/F, LEE GARDEN 3, 1 SUNNING ROAD, CAUSEWAY BAY, HONG KONG

Legal Classification

Not A Poison

Sale Requirement*

Over-The-Counter Medicines

Ingredients

Active Ingredient
arginine (as hydrochloride)
biotin
calcium glycerophosphate
calcium pantothenate
choline bitartrate
colecalciferol
copper sulfate pentahydrate
cyanocobalamin
dextrin
folic acid
gelatin hydrolysate
histidine hydrochloride
isoleucine
leucine
lysine hydrochloride
magnesium sulphate heptahydrate
manganese sulfate monohydrate
nicotinic acid
phytomenadione
potassium acetate
potassium chloride
potassium dihydrogen phosphate
potassium iodide
pyridoxine hydrochloride
riboflavin
rice bran oil
sodium ascorbate
sodium ferrous citrate
thiamine hydrochloride
threonine
tryptophan
valine
vitamin A
vitamin E (as dl-alpha tocoferil acetate)
zinc sulfate heptahydrate

Date of Registration#

14 Apr, 2006

Notes:

	There is news related to local recall of this product within six months. For more details, please click the red flag of the product.
♎	The product is conditionally approved with very limited safety, efficacy, and quality data for public health emergency to satisfy local unmet medical need and the registration status is subjected to be reviewed by the Pharmacy and Poisons (Registration of Pharmaceutical Products and Substances: Certification of Clinical Trial/Medicinal Test) Committee. The product can only be supplied to institutions or registered medical practitioners.
♓	The product is conditionally approved with limited safety, efficacy, and quality data for public health emergency to satisfy local unmet medical need and the registration status is subjected to be reviewed by the Pharmacy and Poisons (Registration of Pharmaceutical Products and Substances: Certification of Clinical Trial/Medicinal Test) Committee. The product can only be supplied to institutions or registered medical practitioners.
♇	The product can only be supplied to institutions or registered medical practitioners.
♐	The application for registration of the product was accepted and evaluated via the "1+" mechanism.
♐♇	The application for registration of the product was accepted and evaluated via the "1+" mechanism. ✝The product can only be supplied to institutions or registered medical practitioners.
Δ	The product is an advanced therapy product (ATP).

*	-Prescription Only Medicines are medicines which must only be purchased with a prescription in a pharmacy.
	-Pharmacy Only Medicines are medicines which can be purchased in a pharmacy in the presence and under the supervision of a registered pharmacist, but without the need of a prescription.
	-Over-the-Counter Medicines are in general medicines classified as Part 2 poison and 'Not a Poison'. For medicines which are classified as 'Not a Poison', they can be freely purchased from a pharmacy (Authorized Seller of Poisons), a medicine store (Listed Seller of Poisons), or any other non-licensed premises; whereas for Part 2 Poisons, they can be purchased only from a pharmacy or a medicine store.

	- For details of legal classification of medicines and sales requirements, please refer to answers to Q5 and Q22 under the FAQs page for the Consumer.


#	Generally, the Pharmacy and Poisons Board issues a registration certificate with a validity period of 5 years, and may be renewed for the same validity period thereafter subject to meeting conditions as stipulated in Pharmacy and Poisons Regulation (Cap 138A) reg 36(7).