"70518-2317-1" National Drug Code (NDC)

Escitalopram 30 TABLET, FILM COATED in 1 BLISTER PACK (70518-2317-1)
(REMEDYREPACK INC.)

NDC Code70518-2317-1
Package Description30 TABLET, FILM COATED in 1 BLISTER PACK (70518-2317-1)
Product NDC70518-2317
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameEscitalopram
Non-Proprietary NameEscitalopram
Dosage FormTABLET, FILM COATED
UsageORAL
Start Marketing Date20190909
Marketing Category NameANDA
Application NumberANDA078032
ManufacturerREMEDYREPACK INC.
Substance NameESCITALOPRAM OXALATE
Strength20
Strength Unitmg/1
Pharmacy ClassesSerotonin Reuptake Inhibitor [EPC], Serotonin Uptake Inhibitors [MoA]

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