BONDRONAT

This brand name is authorized in Austria, Australia, Germany, Ecuador, Estonia, Spain, France, Hong Kong, Croatia, Ireland, Lithuania, Netherlands, Poland, Singapore, Turkey, United Kingdom, South Africa

Active ingredients

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

1 Ibandronic acid
UNII J12U072QL0 - IBANDRONATE SODIUM

Ibandronic acid belongs to the bisphosphonate group of compounds which act specifically on bone. Their selective action on bone tissue is based on the high affinity of bisphosphonates for bone mineral. Bisphosphonates act by inhibiting osteoclast activity, although the precise mechanism is still not clear. In vivo, ibandronic acid prevents experimentally-induced bone destruction caused by cessation of gonadal function, retinoids, tumours or tumour extracts.

Read about Ibandronic acid

Medication package inserts

Below package inserts are available for further reading:

Title Information Source Document Type  
BONDRONAT Film-coated tablets European Medicines Agency (EU) MPI, EU: SmPC
BONDRONAT Concentrate for solution for infusion European Medicines Agency (EU) 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
M05BA06 Ibandronic acid M Musculo-skeletal system → M05 Drugs for treatment of bone diseases → M05B Drugs affecting bone structure and mineralization → M05BA Bisphosphonates
Discover more medicines within M05BA06

Authorization and marketing

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

Country Identification scheme Identifier(s)
Country: AU Pharmaceutical Benefits Scheme Identifier(s): 5750P, 9357L, 9619G
Country: DE Bundesinstitut für Arzneimittel und Medizinprodukte Identifier(s): 00024213, 00283222, 03321176, 03323123, 03422635, 05891475, 05891481, 09384516, 09505227, 09620460, 09686192, 10385567, 10402550, 13916717, 15608776, 16160160, 16804338, 17936852
Country: EC Agencia Nacional de Regulación, Control y Vigilancia Sanitaria Identifier(s): 23.815-1-04-11
Country: EE Ravimiamet Identifier(s): 1173147, 1173158, 1173169, 1173170, 1173181, 1207987
Country: ES Centro de información online de medicamentos de la AEMPS Identifier(s): 96012009
Country: FR Base de données publique des médicaments Identifier(s): 61213881, 64530520
Country: GB Medicines & Healthcare Products Regulatory Agency Identifier(s): 109260, 75402, 75422
Country: HK Department of Health Drug Office Identifier(s): 42670, 52681, 52770, 61449
Country: LT Valstybinė vaistų kontrolės tarnyba Identifier(s): 1027764, 1027766, 1027767, 1027768, 1027769, 1027770
Country: NL Z-Index G-Standaard, PRK Identifier(s): 76945
Country: PL Rejestru Produktów Leczniczych Identifier(s): 100125388, 100125402, 100125419
Country: SG Health Sciences Authority Identifier(s): 11206P, 13425P
Country: TR İlaç ve Tıbbi Cihaz Kurumu Identifier(s): 8699543091815, 8699543091822, 8699543760032, 8699543760056
Country: ZA Health Products Regulatory Authority Identifier(s): 32/3.2/0114, A38/3.2/0381, A38/3.2/0562

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