"68001-196-03" National Drug Code (NDC)

Escitalopram 500 TABLET, FILM COATED in 1 BOTTLE (68001-196-03)
(BluePoint Laboratories)

NDC Code68001-196-03
Package Description500 TABLET, FILM COATED in 1 BOTTLE (68001-196-03)
Product NDC68001-196
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameEscitalopram
Non-Proprietary NameEscitalopram Oxalate
Dosage FormTABLET, FILM COATED
UsageORAL
Start Marketing Date20140206
End Marketing Date20240131
Marketing Category NameANDA
Application NumberANDA202280
ManufacturerBluePoint Laboratories
Substance NameESCITALOPRAM OXALATE
Strength10
Strength Unitmg/1
Pharmacy ClassesSerotonin Reuptake Inhibitor [EPC], Serotonin Uptake Inhibitors [MoA]

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