Combination Vaccines

Multi-antigen vaccines combining protection against two or more diseases in a single product

This page catalogs 34 combination vaccine products spanning currently US-licensed DTaP, Tdap, MMR, MMRV, and hexavalent formulations, European equivalents, WHO-prequalified pentavalent products, and discontinued predecessors. Combination vaccines reduce the number of injections required, improving immunization compliance and coverage. This is the largest single category in the Vaccine Catalog.

Last updated: April 2026.

Combination Vaccine Catalog

Trade Name Generic Designation Manufacturer Vaccine Type Regulatory Status & Year Key Notes
Daptacel DTaP (diphtheria, tetanus, acellular pertussis) Sanofi Pasteur Toxoid + acellular FDA Licensed, 2002 Pediatric DTaP
Infanrix DTaP GSK Toxoid + acellular FDA Licensed, 1997 Pediatric DTaP
Adacel Tdap (tetanus, diphtheria, acellular pertussis) Sanofi Pasteur Toxoid + acellular FDA Licensed, 2005 Adolescent/adult booster
Boostrix Tdap GSK Toxoid + acellular FDA Licensed, 2005 Adolescent/adult booster; maternal use
Tenivac Td (tetanus + diphtheria adult) Sanofi Pasteur Toxoid FDA Licensed Adult Td booster
TDVAX Td (tetanus + diphtheria adult) MassBiologics Toxoid FDA Licensed Adult Td
M-M-R II Measles, mumps, rubella Merck Live-attenuated viral FDA Licensed, 1978 Standard MMR
Priorix Measles, mumps, rubella GSK Live-attenuated viral FDA Licensed, 2022 Second US MMR
ProQuad MMRV (measles, mumps, rubella, varicella) Merck Live-attenuated viral FDA Licensed, 2005 4-in-1 MMRV
Pediarix DTaP-HepB-IPV GSK Combination FDA Licensed, 2002 5-in-1 pediatric
Pentacel DTaP-IPV/Hib Sanofi Pasteur Combination FDA Licensed, 2008 5-in-1 with Hib
Kinrix DTaP-IPV GSK Combination FDA Licensed, 2008 4-in-1 booster
Quadracel DTaP-IPV Sanofi Pasteur Combination FDA Licensed, 2015 4-in-1 booster
Vaxelis DTaP-IPV-Hib-HepB MSP Vaccine Co (Merck/Sanofi) Combination FDA Licensed, 2018 6-in-1 hexavalent
Infanrix Hexa DTaP-IPV-Hib-HepB GSK Combination EMA Authorized GSK hexavalent; not US-licensed
Hexaxim / Hexyon DTaP-IPV-Hib-HepB Sanofi Pasteur Combination EMA Authorized Sanofi hexavalent; not US-licensed
Twinrix Hepatitis A + Hepatitis B GSK Inactivated + Recombinant FDA Licensed, 2001 Combination Hep A/B adult
Penbraya MenABCWY Pfizer Conjugate + recombinant FDA Licensed, 2023 First pentavalent meningococcal
Penmenvy MenABCWY Sanofi Conjugate + recombinant FDA Licensed, 2025 Second pentavalent meningococcal
Trihibit DTaP/Hib Sanofi Pasteur Combination FDA Licensed; Discontinued Discontinued combination
Tri-Immunol DTP (whole-cell pertussis) Wyeth-Lederle Toxoid + killed bacterial FDA Licensed; Discontinued Whole-cell DTP; replaced by DTaP
Tripedia DTaP Sanofi Pasteur (Aventis) Toxoid + acellular FDA Licensed, 1992; Discontinued Early acellular pertussis
ACEL-IMUNE DTaP Wyeth-Lederle Toxoid + acellular FDA Licensed; Discontinued Early DTaP
Certiva DTaP North American Vaccine Toxoid + acellular FDA Licensed; Discontinued Single pertussis antigen DTaP
Biavax Rubella-Mumps vaccine Merck Live-attenuated viral FDA Licensed; Discontinued MR combination; replaced by MMR
Pluserix MMR vaccine SKB/GSK Live-attenuated viral Licensed (non-US); Withdrawn Urabe mumps strain; withdrawn after meningitis signal
Pediace DTaP-IPV-Hib Sanofi Pasteur Combination Licensed (non-US) Canadian/EU 5-in-1
Quinvaxem DTP-HepB-Hib pentavalent Novartis/Biological E Whole-cell combination WHO Prequalified; Discontinued WHO-prequalified pentavalent for GAVI
Repevax Tdap-IPV Sanofi Pasteur Combination Licensed (EU) European Tdap-IPV booster
Tri-Solgen DTP (whole-cell) Wyeth Toxoid + killed bacterial Discontinued Historical whole-cell DTP
Tri-Immunol (alt) DTP (whole-cell) Lederle Toxoid + killed bacterial Discontinued Lederle whole-cell DTP
Trivax DTP (whole-cell) Wellcome Toxoid + killed bacterial Discontinued UK whole-cell DTP
Refortrix Tdap GSK Toxoid + acellular Licensed (non-US) European Tdap booster
Revaxis Td-IPV (tetanus-diphtheria-polio) Sanofi Pasteur Toxoid + inactivated Licensed (EU) European Td-IPV adult booster

Sources

Regulatory data sourced from FDA CBER Vaccines Licensed for Use in the United States (March 2026), EMA Medicines database, and WHO Prequalified Vaccines list. Historical context informed by Khan, Shaz, The Ultimate Vaccine Timeline.

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