This brand name is authorized in Cyprus, Germany, Estonia, Finland, Ireland, Israel, Malta, Romania, Singapore, United Kingdom, United States
The drug BINOSTO contains one active pharmaceutical ingredient (API):
1
Alendronate sodium trihydrate
UNII 2UY4M2U3RA - ALENDRONATE SODIUM
|
Alendronic acid is a bisphosphonate that inhibits osteoclastic bone resorption with no direct effect on bone formation. The bone formed during treatment with alendronic acid is of normal quality. |
Below package inserts are available for further reading:
Title | Information Source | Document Type | |
---|---|---|---|
BINOSTO Effervescent tablet | Marketing Authorisation Holder | MPI, EU: SmPC |
This drug has been classified in the anatomical therapeutic chemical (ATC) classification system as follows:
ATC code | Group title | Classification |
---|---|---|
M05BA04 | Alendronic acid | M Musculo-skeletal system → M05 Drugs for treatment of bone diseases → M05B Drugs affecting bone structure and mineralization → M05BA Bisphosphonates |
This drug has been assigned below unique identifiers within the countries it is being marketed:
Country | Identification scheme | Identifier(s) |
---|---|---|
Country: DE | Bundesinstitut für Arzneimittel und Medizinprodukte | Identifier(s): 12592537, 12592543 |
Country: EE | Ravimiamet | Identifier(s): 1647604, 1647615 |
Country: FI | Lääkealan turvallisuus- ja kehittämiskeskus | Identifier(s): 529117 |
Country: GB | Medicines & Healthcare Products Regulatory Agency | Identifier(s): 303174, 381207, 391001 |
Country: IE | Health Products Regulatory Authority | Identifier(s): 37011 |
Country: IL | מִשְׂרַד הַבְּרִיאוּת | Identifier(s): 8054 |
Country: MT | Medicines Authority | Identifier(s): AA1173/06801 |
Country: RO | Agenția Națională a Medicamentului și a Dispozitivelor Medicale | Identifier(s): W63265001, W63265002, W63265003 |
Country: SG | Health Sciences Authority | Identifier(s): 15268P |
Country: US | FDA, National Drug Code | Identifier(s): 17139-400 |
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