Kinrix
Diphtheria and Tetanus Toxoids and Acellular Pertussis Adsorbed and Inactivated Poliovirus Vaccine · Injection, Suspension · Intramuscular
No FDA structured label text is available for Kinrix. The NDC listings below come from the FDA National Drug Code directory.
Active ingredients
- Corynebacterium Diphtheriae Toxoid Antigen (formaldehyde Inactivated) in 1 product
- Clostridium Tetani Toxoid Antigen (formaldehyde Inactivated) in 1 product
- Bordetella Pertussis Filamentous Hemagglutinin Antigen (formaldehyde Inactivated) in 1 product
- Bordetella Pertussis Pertactin Antigen (formaldehyde Inactivated) in 1 product
- Bordetella Pertussis Toxoid Antigen (formaldehyde, Glutaraldehyde Inactivated) in 1 product
- Poliovirus Type 1 Antigen (formaldehyde Inactivated) in 1 product
- Poliovirus Type 2 Antigen (formaldehyde Inactivated) in 1 product
- Poliovirus Type 3 Antigen (formaldehyde Inactivated) in 1 product
Kinrix NDC products (1)
| NDC | Strength & form | Labeler | Type |
|---|---|---|---|
| 58160-812 | Corynebacterium Diphtheriae Toxoid Antigen (formaldehyde Inactivated) 25 [iU]/.5mL; Clostridium Tetani Toxoid Antigen… Injection, Suspension | GlaxoSmithKline Biologicals SA | BLA |
Frequently asked questions
Who makes Kinrix?
Kinrix is listed by 1 labeler in the FDA NDC directory, including GlaxoSmithKline Biologicals SA.