"72000-310-06" National Drug Code (NDC)

Sivextro 1 BLISTER PACK in 1 CARTON (72000-310-06) > 6 TABLET, FILM COATED in 1 BLISTER PACK
(Nabriva Therapeutics US, Inc.)

NDC Code72000-310-06
Package Description1 BLISTER PACK in 1 CARTON (72000-310-06) > 6 TABLET, FILM COATED in 1 BLISTER PACK
Product NDC72000-310
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameSivextro
Non-Proprietary NameTedizolid Phosphate
Dosage FormTABLET, FILM COATED
UsageORAL
Start Marketing Date20140620
Marketing Category NameNDA
Application NumberNDA205435
ManufacturerNabriva Therapeutics US, Inc.
Substance NameTEDIZOLID PHOSPHATE
Strength200
Strength Unitmg/1
Pharmacy ClassesBreast Cancer Resistance Protein Inhibitors [MoA], Oxazolidinone Antibacterial [EPC], Oxazolidinones [CS]

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