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ACTEMRA - tocilizumab

Navigation: NDC > Supplier starting with: G > GENENTECH, INC.
Field Value
NDC Code: 50242-136
Proprietary Name: ACTEMRA
Suffix:
Non-Proprietary Name: tocilizumab
Dosage Form: INJECTION, SOLUTION, CONCENTRATE
Method: INTRAVENOUS
Original Marketing Date: 08-01-2010
Category Name: BLA
Application Number: BLA125276
Labeler: GENENTECH, INC.
Substance Name: TOCILIZUMAB
Active Numerator Strength: 20
Active Ingredient Unit: mg/mL
Pharm Classes:
DEA Schedule: