Product Details for: Varivax

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Product Number
Dosage Form
Route of Administration
Strength
Product Presentation
License Type
Proprietary Name
Marketing Status
001
For Injection
Subcutaneous
NLT 1350PFU/.5ML
Single-Dose Vial
351(a)
Varivax
Rx
002
For Injection
Intramuscular
NLT 1350PFU/.5ML
Single-Dose Vial
351(a)
Varivax
Rx
Proper Name
Varicella Virus Vaccine Live
BLA Number
103552
Applicant
Merck Sharp & Dohme LLC
Original Approval Date
March 17, 1995
Date of First Licensure
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