OSTEOFLEX ULTRA

This brand name is authorized in Nigeria.

Active ingredients

The drug OSTEOFLEX ULTRA contains one active pharmaceutical ingredient (API):

1	Hyaluronate sodium UNII S270N0TRQY - HYALURONIC ACID
	Read more about Hyaluronate sodium

Packages

This drug has been approved in Nigeria as follows:

Identifier	Form	Presentation	Description	Approval
A11-100699	Caplet	OSTEOFLEX ULTRA CAPLET TAB 158	36 NF-PP-388982 OSTEOFLEX ULTRA CAPLET HYALURONIC ACID, CARTILAGE BLEND, BORON A11-100699 Drugs MUSCULO-SKELETAL SYSTEM Nigerian Products 158 Over The Counter (OTC) 11/24/2023 UNITED AFRICAN LABORATORY LIMITED, TEBUN BISIRIYU STREET, SHASHA, LAGOS IKEJA LAGOS 8181519968 ualafrica@yahoo.com ECOMED PHARMA LIMIED, PLOT 32, LYNSON CHEMICAL AVENUE, KM 38, LAGOS ABEOKUTA, SANGO OTA, OGUN STATE., Nigeria	30/04/2024

Medicine classification

This drug has been classified in the anatomical therapeutic chemical (ATC) classification system as follows:

ATC Group		Classification
M09AX01	Hyaluronic acid	M Musculo-skeletal system → M09 Other drugs for disorders of the musculo-skeletal system → M09A Other drugs for disorders of the musculo-skeletal system → M09AX Other drugs for disorders of the musculo-skeletal system
Discover more medicines within M09AX01

Authorization and marketing

This drug has been assigned below unique identifiers within the countries it is being marketed:

Country	Identification scheme	Identifier(s)
NG	Registered Drug Product Database	A11-100699