"72000-110-10" National Drug Code (NDC)

Xenleta 10 TABLET, COATED in 1 BLISTER PACK (72000-110-10)
(Nabriva Therapeutics US, Inc.)

NDC Code72000-110-10
Package Description10 TABLET, COATED in 1 BLISTER PACK (72000-110-10)
Product NDC72000-110
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameXenleta
Non-Proprietary NameLefamulin Acetate
Dosage FormTABLET, COATED
UsageORAL
Start Marketing Date20190909
Marketing Category NameNDA
Application NumberNDA211672
ManufacturerNabriva Therapeutics US, Inc.
Substance NameLEFAMULIN ACETATE
Strength600
Strength Unitmg/1
Pharmacy ClassesCytochrome P450 3A Inhibitors [MoA], Cytochrome P450 3A4 Inhibitors [MoA], Diterpenes [CS], Pleuromutilin Antibacterial [EPC]

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