Product Details for: Tubersol

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Product Number
Dosage Form
Route of Administration
Strength
Product Presentation
License Type
Proprietary Name
Marketing Status
001
Injection
Intradermal
5TU/.1ML
Multi-Dose Vial
351(a)
Tubersol
Rx
Proper Name
Tuberculin, Purified Protein Derivative
BLA Number
103941
Applicant
Sanofi Vaccines Canada Ltd.
Original Approval Date
February 24, 2000
Date of First Licensure
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