Overview
Poliovirus type 2 antigen is a suspension of poliovirus Type 2 (MEF-1) 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 2. The vaccine contains purified and inactivated poliovirus type 2 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 2
Clinical Trials
Title | Posted | Study ID | Phase | Status | Sponsor |
|---|
No clinical trials found
No clinical trials found for this drug
FDA Drug Approvals
Approved Product | Manufacturer | NDC Code | Route | Strength | Effective Date |
|---|---|---|---|---|---|
| A-S Medication Solutions | 50090-7541 | INTRAMUSCULAR | 8 [iU] in 0.5 mL | 8/13/2025 | |
| GlaxoSmithKline Biologicals SA | 58160-812 | INTRAMUSCULAR | 8 [iU] in 0.5 mL | 11/26/2024 |
EMA Drug Approvals
Approved Product | Authorization Holder | Status | Issued Date |
|---|---|---|---|
| No EMA approvals found for this drug. | |||
HSA Drug Approvals
Approved Product | Manufacturer | Approval Number | Dosage Form | Strength | Approval Date |
|---|---|---|---|---|---|
| HEXAXIM SUSPENSION FOR INJECTION IN PRE-FILLED SYRINGE | SIN14834P | INJECTION, SUSPENSION | 40 DU/0.5 mL | 8/25/2015 | |
| HEXAXIM SUSPENSION FOR INJECTION IN PRE-FILLED SYRINGE | SIN14834P | INJECTION, SUSPENSION | 8 DU/0.5 mL | 8/25/2015 | |
| INFANRIX HEXA VACCINE | SIN12288P | INJECTION | 8 du/0.5 ml | 5/7/2003 | |
| BOOSTRIX POLIO SUSPENSION FOR INJECTION | SIN15888P | INJECTION, SUSPENSION | 8 DU/0.5 ml | 2/20/2020 | |
| Tetraxim Vaccine | SIN15026P | INJECTION, SUSPENSION | 8 DU/0.5ml | 6/6/2016 |
NMPA Drug Approvals
Approved Product | Company | Approval Number | Drug Type | Dosage Form | Approval Date |
|---|---|---|---|---|---|
| No NMPA approvals found for this drug. | |||||
PPB Drug Approvals
Approved Product | Registration No. | Company | Licence No. | Strength | Registration Date |
|---|---|---|---|---|---|
| No PPB approvals found for this drug. | |||||
TGA Drug Approvals
Approved Product | ARTG ID | Sponsor | Registration Type | Status | Registration Date |
|---|---|---|---|---|---|
| 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 | 8 UNIT / 0.5 ML | 10/25/2012 | |
| INACTIVATED POLIOMYELITIS VACCINE (DIPLOID CELL ORIGIN) - IPV | 02231267 | Solution - Subcutaneous | 8 UNIT / 0.5 ML | 11/17/1998 | |
| PEDIACEL | 02243167 | Suspension - Intramuscular | 7 UNIT / 0.5 ML | 10/4/2007 | |
| BOOSTRIX-POLIO | 02312557 | Suspension - Intramuscular | 8 D / 0.5 ML | 10/22/2010 | |
| QUADRACEL | 02230946 | Suspension - Intramuscular | 8 UNIT / 0.5 ML | 6/20/1997 | |
| INFANRIX-IPV/HIB | 02257122 | Suspension - Intramuscular | 8 UNIT / 0.5 ML | 10/25/2012 | |
| PENTACEL | 02231343 | Powder For Solution
,
Liquid - Intramuscular | 8 UNIT / 0.5 ML | 6/16/1997 | |
| TD POLIO ADSORBED | 00615358 | Suspension - Intramuscular | 8 UNIT / 0.5 ML | 12/31/1984 | |
| DT POLIO ADSORBED - SUS IM | aventis pasteur limited | 02189127 | Suspension - Intramuscular | 8 UNIT / 0.5 ML | 12/12/1996 |
CIMA AEMPS Drug Approvals
Approved Product | Company | Registration Number | Pharmaceutical Form | Prescription Type | Status |
|---|---|---|---|---|---|
| No CIMA AEMPS (Spain) approvals found for this drug. | |||||
Philippines FDA Drug Approvals
Approved Product | Company | License Number | Dosage Form | Strength | Approval Date |
|---|---|---|---|---|---|
| No Philippines FDA approvals found for this drug. | |||||
Saudi SFDA Drug Approvals
Approved Product | Company | License Number | Dosage Form | Strength | Approval Date |
|---|---|---|---|---|---|
| No Saudi SFDA approvals found for this drug. | |||||
Malaysia NPRA Drug Approvals
Approved Product | Company | Registration Number | Dosage Form | Strength | Approval Date |
|---|---|---|---|---|---|
| No Malaysia NPRA approvals found for this drug. | |||||
UK EMC Drug Information
Medicine Name | MA Holder | MA Number | Pharmaceutical Form | Active Ingredient | Authorization Date |
|---|---|---|---|---|---|
| No UK EMC drug information found for this drug. | |||||
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