Drugplain

VARIVAX 1350 [PFU]/.5mL

Varicella Virus Vaccine Live · INJECTION, POWDER, LYOPHILIZED, FOR SUSPENSION · Merck Sharp & Dohme LLC

No Recall History
Plain English

VARIVAX is a injection, powder, lyophilized, for suspension containing varicella virus vaccine live at 1350 [PFU]/.5mL, taken subcutaneous. Manufactured by Merck Sharp & Dohme LLC.

Key Facts

Brand Name
VARIVAX
Generic Name
Varicella Virus Vaccine Live
NDC Code (Product)
0006-4827
Manufacturer
Merck Sharp & Dohme LLC
Strength
1350 [PFU]/.5mL
Dosage Form
INJECTION, POWDER, LYOPHILIZED, FOR SUSPENSION
Route
SUBCUTANEOUS
Marketing Status
Application #
BLA103552
Marketing Start
03/17/1995

Recall History

No Recall History

Frequently Asked Questions

What is VARIVAX used for?

VARIVAX contains Varicella Virus Vaccine Live. It is a injection, powder, lyophilized, for suspension taken subcutaneous. Consult your doctor for specific uses.

Is VARIVAX a controlled substance?

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

What is the generic name for VARIVAX?

The generic name for VARIVAX is Varicella Virus Vaccine Live. There are no other listed brand versions of Varicella Virus Vaccine Live.

What is the NDC code for VARIVAX 1350 [PFU]/.5mL?

The NDC (National Drug Code) for VARIVAX 1350 [PFU]/.5mL is 0006-4827, listed by Merck Sharp & Dohme LLC.

Product NDC

0006-4827

Package NDC

0006-4827-00

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

Data from openFDA · Public domain (CC0 1.0)