NUROMAX

This brand name is authorized in Nigeria.

Active ingredients

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

1	Pregabalin UNII 55JG375S6M - PREGABALIN
	Pregabalin binds to an auxiliary subunit (α2-δ protein) of voltage-gated calcium channels in the central nervous system.
	Read more about Pregabalin

Packages

This drug has been approved in Nigeria as follows:

Identifier	Form	Presentation	Description	Approval
A4-100723	Capsule	Nuromax 75 Capsule CAP 75 mg 3 x 10's (in Alu-Alu blisters)	Hard Gelatin Capsule Red/white size "4" capsule containing white color powder 9 NF-PP-351915 NUROMAX 75 CAPSULE Pregabalin 75 mg Pregabalin 75 mg, Lactose, Pre Gelatinized Starch, Purified Water, Cross Carmellose Sodium (Vivasole), Purified Talc, E.H.G. A4-100723 Drugs Imported Products 310 Prescription Only Medicine (POM) 8/15/2023 SJS LIFE SCIENCES LIMITED, 11, OLU AKERELE STREET, IKEJA, LAGOS 8114441430 sjslifesciencesltd@gmail.com GLOBELA PHARMA PVT. LTD., 357 358, G.I.D.C., SACHIN, SURAT - 394 230, GUJARAT, INDIA, India	31/01/2024

Medicine classification

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

ATC Group		Classification
N02BF02	Pregabalin	N Nervous system → N02 Analgesics → N02B Other analgesics and antipyretics → N02BF Gabapentinoids
Discover more medicines within N02BF02

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	A4-100723