Drugplain

TWINRIX 720 [iU]/mL

Hepatitis A and Hepatitis B (Recombinant) Vaccine · INJECTION, SUSPENSION · GlaxoSmithKline Biologicals SA

No Recall History
Plain English

TWINRIX is a injection, suspension containing hepatitis a and hepatitis b (recombinant) vaccine at 720 [iU]/mL, taken intramuscular. Manufactured by GlaxoSmithKline Biologicals SA.

Key Facts

Brand Name
TWINRIX
Generic Name
Hepatitis A and Hepatitis B (Recombinant) Vaccine
NDC Code (Product)
58160-815
Manufacturer
GlaxoSmithKline Biologicals SA
Strength
720 [iU]/mL
Dosage Form
INJECTION, SUSPENSION
Route
INTRAMUSCULAR
Marketing Status
Application #
BLA103850
Marketing Start
06/07/2007

Recall History

No Recall History

Frequently Asked Questions

What is TWINRIX used for?

TWINRIX contains Hepatitis A and Hepatitis B (Recombinant) Vaccine. It is a injection, suspension taken intramuscular. Consult your doctor for specific uses.

Is TWINRIX a controlled substance?

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

What is the generic name for TWINRIX?

The generic name for TWINRIX is Hepatitis A and Hepatitis B (Recombinant) Vaccine. There are no other listed brand versions of Hepatitis A and Hepatitis B (Recombinant) Vaccine.

What is the NDC code for TWINRIX 720 [iU]/mL?

The NDC (National Drug Code) for TWINRIX 720 [iU]/mL is 58160-815, listed by GlaxoSmithKline Biologicals SA.

Product NDC

58160-815

Package NDC

58160-815-52

Other TWINRIX Dosages

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

Data from openFDA · Public domain (CC0 1.0)