Overview
Poliovirus type 1 antigen is a suspension of poliovirus Type 1 (Mahoney) used in the active immunization of infants (as young as 6 weeks of age), children, and adults for the prevention of poliomyelitis caused by poliovirus Type 1. The vaccine contains purified and inactivated poliovirus type 1 that were grown from a continuous line of monkey kidney cells.
Indication
No indication information available.
Associated Conditions
- Poliomyelitis caused by Poliovirus
- Poliomyelitis caused by poliovirus type 1
Clinical Trials
Title | Posted | Study ID | Phase | Status | Sponsor |
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No clinical trials found
No clinical trials found for this drug
FDA Drug Approvals
Approved Product | Manufacturer | NDC Code | Route | Strength | Effective Date |
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GlaxoSmithKline Biologicals SA | 58160-812 | INTRAMUSCULAR | 40 [iU] in 0.5 mL | 11/26/2024 |
EMA Drug Approvals
Approved Product | Authorization Holder | Status | Issued Date |
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No EMA approvals found for this drug. |
HSA Drug Approvals
Approved Product | Manufacturer | Approval Number | Dosage Form | Strength | Approval Date |
---|---|---|---|---|---|
INFANRIX HEXA VACCINE | SIN12288P | INJECTION | 40 du/0.5 ml | 5/7/2003 | |
Tetraxim Vaccine | SIN15026P | INJECTION, SUSPENSION | 40 DU/0.5ml | 6/6/2016 |
NMPA Drug Approvals
Approved Product | Company | Approval Number | Drug Type | Dosage Form | Approval Date |
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No NMPA approvals found for this drug. |
PPB Drug Approvals
Approved Product | Registration No. | Company | Licence No. | Strength | Registration Date |
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No PPB approvals found for this drug. |
TGA Drug Approvals
Approved Product | ARTG ID | Sponsor | Registration Type | Status | Registration Date |
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No TGA approvals found for this drug. |
Health Canada Drug Approvals
Approved Product | Company | DIN | Dosage Form | Strength | Market Date |
---|---|---|---|---|---|
INFANRIX-IPV | 02241284 | Suspension - Intramuscular | 40 UNIT / 0.5 ML | 10/25/2012 | |
PEDIACEL | 02243167 | Suspension - Intramuscular | 29 UNIT / 0.5 ML | 10/4/2007 | |
BOOSTRIX-POLIO | 02312557 | Suspension - Intramuscular | 40 D / 0.5 ML | 10/22/2010 | |
INFANRIX-IPV/HIB | 02257122 | Suspension - Intramuscular | 40 UNIT / 0.5 ML | 10/25/2012 |
CIMA AEMPS Drug Approvals
Approved Product | Company | Registration Number | Pharmaceutical Form | Prescription Type | Status |
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No CIMA AEMPS (Spain) approvals found for this drug. |
Philippines FDA Drug Approvals
Approved Product | Company | License Number | Dosage Form | Strength | Approval Date |
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No Philippines FDA approvals found for this drug. |
Saudi SFDA Drug Approvals
Approved Product | Company | License Number | Dosage Form | Strength | Approval Date |
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No Saudi SFDA approvals found for this drug. |
Malaysia NPRA Drug Approvals
Approved Product | Company | Registration Number | Dosage Form | Strength | Approval Date |
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No Malaysia NPRA approvals found for this drug. |
UK EMC Drug Information
Medicine Name | MA Holder | MA Number | Pharmaceutical Form | Active Ingredient | Authorization Date |
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No UK EMC drug information found for this drug. |
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