This brand name is authorized in Austria, Cyprus, Estonia, Finland, France, Hong Kong SAR China, Netherlands, New Zealand, Poland, Turkey.
The drug ACT-HIB contains one active pharmaceutical ingredient (API):
1
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UNII
FLV5I5W26R - HAEMOPHILUS INFLUENZAE TYPE B STRAIN 1482 CAPSULAR POLYSACCHARIDE TETANUS TOXOID CONJUGATE ANTIGEN
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Haemophilus influenza type B (Hib) is a bacteria responsible for severe pneumonia, meningitis and other invasive diseases almost exclusively in young children. Vaccines are the only public health tool capable of preventing the majority of serious Hib disease. |
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This drug has been classified in the anatomical therapeutic chemical (ATC) classification system as follows:
| ATC Group | Classification | |
|---|---|---|
| J07AG01 | Haemophilus influenzae B, purified antigen conjugated | J Antiinfectives for systemic use → J07 Vaccines → J07A Bacterial vaccines → J07AG Haemophilus influenzae B vaccines |
This drug has been assigned below unique identifiers within the countries it is being marketed:
| Country | Identification scheme | Identifier(s) |
|---|---|---|
| EE | Ravimiamet | 1019584 |
| FI | Lääkealan turvallisuus- ja kehittämiskeskus | 198901 |
| FR | Base de données publique des médicaments | 61104024 |
| HK | Department of Health Drug Office | 37568 |
| NL | Z-Index G-Standaard | 13901397 |
| NL | Z-Index G-Standaard, PRK | 36471 |
| NZ | Medicines and Medical Devices Safety Authority | 6803 |
| PL | Rejestru Produktów Leczniczych | 100224400 |
| TR | İlaç ve Tıbbi Cihaz Kurumu | 8699625960022 |
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