"70518-1942-2" National Drug Code (NDC)

Acyclovir 21 TABLET in 1 BOTTLE, PLASTIC (70518-1942-2)
(REMEDYREPACK INC.)

NDC Code70518-1942-2
Package Description21 TABLET in 1 BOTTLE, PLASTIC (70518-1942-2)
Product NDC70518-1942
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameAcyclovir
Non-Proprietary NameAcyclovir
Dosage FormTABLET
UsageORAL
Start Marketing Date20190307
Marketing Category NameANDA
Application NumberANDA210401
ManufacturerREMEDYREPACK INC.
Substance NameACYCLOVIR
Strength400
Strength Unitmg/1
Pharmacy ClassesDNA Polymerase Inhibitors [MoA], Herpes Simplex Virus Nucleoside Analog DNA Polymerase Inhibitor [EPC], Herpes Zoster Virus Nucleoside Analog DNA Polymerase Inhibitor [EPC], Herpesvirus Nucleoside Analog DNA Polymerase Inhibitor [EPC], Nucleoside Analog [EXT]

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