
Alembic Global Holdings SA has received tentative approval from the US Food and Drug Administration for its abbreviated new drug application (ANDA) Treprostinil Injection in the strengths of 20 mg/20 ml (1 mg/ml), 50 mg/20 ml (2.5 mg/ml), 100 mg/20 ml (5 mg/ml), and 200 mg/20 ml (10 mg/ml), multiple-dose vials, Alembic Pharmaceuticals said in a regulatory filing.
from Healthcare/Biotech-Industry-Economic Times https://ift.tt/3i9ymgM
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