OSPAMOX

This brand name is authorized in Austria, Estonia, Hong Kong, Croatia, Lithuania, Nigeria, New Zealand, Poland, Romania, Singapore

Active ingredients

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

1 Amoxicillin UNII 804826J2HU - AMOXICILLIN

Amoxicillin is a semisynthetic penicillin (beta-lactam antibiotic) that inhibits one or more enzymes (often referred to as penicillin-binding proteins, PBPs) in the biosynthetic pathway of bactericidal peptidoglycan, which is an integral structural component of the bacterial cell wall. Inhibition of peptidoglycan synthesis leads to weakening of the cell wall, which is usually followed by cell lysis and death. Read about Amoxicillin

Medication package inserts

Below package inserts are available for further reading:

Title	Information Source	Document Type
OSPAMOX Powder for oral suspension / Paediatric drops	Medicines and Medical Devices Safety Authority (NZ)	MPI, EU: SmPC

Medicine classification

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

ATC code	Group title	Classification
J01CA04	Amoxicillin	J Antiinfectives for systemic use → J01 Antibacterials for systemic use → J01C Beta-lactam antibacterials, penicillins → J01CA Penicillins with extended spectrum
Discover more medicines within J01CA04

Authorization and marketing

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

Country	Identification scheme	Identifier(s)
Country: EE	Ravimiamet	Identifier(s): 1181999, 1182002, 1306774, 1306785, 1306796, 1306808, 1306819, 1306820, 1306831, 1306842, 1306853, 1306864, 1306875, 1306886, 1306897, 1306909, 1306910, 1306921, 1306932, 1306943, 1306954, 1306965
Country: HK	Department of Health Drug Office	Identifier(s): 32357, 33168
Country: HR	Agencija za lijekove i medicinske proizvode	Identifier(s): HR-H-326396791
Country: LT	Valstybinė vaistų kontrolės tarnyba	Identifier(s): 1005024, 1005025, 1005581, 1005582, 1026247, 1026248, 1026268, 1026272, 1026273, 1026284, 1027094, 1032143, 1032144, 1032145, 1032146, 1032147, 1032148, 1032159, 1032160, 1032161, 1032162, 1032163, 1032164, 1032165, 1032166, 1032167, 1032168, 1032169, 1032170, 1032171, 1032172, 1052833, 1052835, 1052836, 1052837, 1052838, 1052839, 1052840, 1052841, 1052842, 1052844, 1052845, 1052846, 1052847, 1052848, 1052849, 1052850, 1053222, 1053223, 1053224, 1060289, 1093333
Country: NG	Registered Drug Product Database	Identifier(s): B4-3580
Country: NZ	Medicines and Medical Devices Safety Authority	Identifier(s): 8381, 8382, 8723, 8724, 8763, 9763
Country: PL	Rejestru Produktów Leczniczych	Identifier(s): 100049954, 100049960, 100049977, 100157916, 100226468, 100227440, 100229030, 100229047, 100468886
Country: RO	Agenția Națională a Medicamentului și a Dispozitivelor Medicale	Identifier(s): W00388002, W00388003, W41578001, W41578002, W41580002, W41580003, W41600001, W41600002
Country: SG	Health Sciences Authority	Identifier(s): 02350P, 03690P, 03691P