Drugplain

INFANRIX 25 ug/.5mL

Diphtheria and Tetanus Toxoids and Acellular Pertussis Vaccine Adsorbed · SUSPENSION · GlaxoSmithKline Biologicals SA

No Recall History
Plain English

INFANRIX is a suspension containing diphtheria and tetanus toxoids and acellular pertussis vaccine adsorbed at 25 ug/.5mL, taken intramuscular. Manufactured by GlaxoSmithKline Biologicals SA.

Key Facts

Brand Name
INFANRIX
Generic Name
Diphtheria and Tetanus Toxoids and Acellular Pertussis Vaccine Adsorbed
NDC Code (Product)
58160-810
Manufacturer
GlaxoSmithKline Biologicals SA
Strength
25 ug/.5mL
Dosage Form
SUSPENSION
Route
INTRAMUSCULAR
Marketing Status
Application #
BLA103647
Marketing Start
07/24/2009

Recall History

No Recall History

Frequently Asked Questions

What is INFANRIX used for?

INFANRIX contains Diphtheria and Tetanus Toxoids and Acellular Pertussis Vaccine Adsorbed. It is a suspension taken intramuscular. Consult your doctor for specific uses.

Is INFANRIX a controlled substance?

INFANRIX is not classified as a controlled substance by the DEA.

What is the generic name for INFANRIX?

The generic name for INFANRIX is Diphtheria and Tetanus Toxoids and Acellular Pertussis Vaccine Adsorbed. There are no other listed brand versions of Diphtheria and Tetanus Toxoids and Acellular Pertussis Vaccine Adsorbed.

What is the NDC code for INFANRIX 25 ug/.5mL?

The NDC (National Drug Code) for INFANRIX 25 ug/.5mL is 58160-810, listed by GlaxoSmithKline Biologicals SA.

Product NDC

58160-810

Package NDC

58160-810-52

Not medical advice. Always consult your doctor or pharmacist before making any medication decisions.

Data from openFDA · Public domain (CC0 1.0)