"68462-291-13" National Drug Code (NDC)

Linezolid 3 BLISTER PACK in 1 CARTON (68462-291-13) > 10 TABLET, FILM COATED in 1 BLISTER PACK
(Glenmark Pharmaceuticals Inc., USA)

NDC Code68462-291-13
Package Description3 BLISTER PACK in 1 CARTON (68462-291-13) > 10 TABLET, FILM COATED in 1 BLISTER PACK
Product NDC68462-291
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameLinezolid
Non-Proprietary NameLinezolid
Dosage FormTABLET, FILM COATED
UsageORAL
Start Marketing Date20151221
Marketing Category NameANDA
Application NumberANDA078987
ManufacturerGlenmark Pharmaceuticals Inc., USA
Substance NameLINEZOLID
Strength600
Strength Unitmg/1
Pharmacy ClassesOxazolidinone Antibacterial [EPC],Oxazolidinones [CS]

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