HUMOG

This brand name is authorized in Nigeria.

Active ingredients

The drug HUMOG contains one active pharmaceutical ingredient (API):

1	Menotropin UNII 5Y9QQM372Q - MENOTROPINS
	Read more about Menotropin

Packages

This drug has been approved in Nigeria as follows:

Identifier	Form	Presentation	Description	Approval
A6-0232	Powder for injection	Humog 75 HP INJ_PWD 75 IU 1 x 1's (in vial) + 1 mL Sodium Chloride Injection BP as solvent (in ampoule)	Freeze dried powder for Injection in a vial plus 1 mL Sodium Chloride Injection BP as solvent (in ampoule). White powder or cake	18/12/2024
A6-0233	Powder for injection	Humog 150 HP Injection INJ_PWD 150 IU 1 x 1's (in vial) + 1 mL Sodium Chloride Injection BP as solvent (in ampoule)	Freeze dried powder for Injection in a vial plus 1 mL of Sodium Chloride Injection BP as diluent in an ampoule. White powder or cake	18/12/2024

Medicine classification

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

ATC Group		Classification
G03GA02	Human menopausal gonadotrophin	G Genito urinary system and sex hormones → G03 Sex hormones and modulators of the genital system → G03G Gonadotropins and other ovulation stimulants → G03GA Gonadotropins
Discover more medicines within G03GA02

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	A6-0232, A6-0233