"70518-2032-0" National Drug Code (NDC)

Acyclovir 30 TABLET in 1 BLISTER PACK (70518-2032-0)
(REMEDYREPACK INC.)

NDC Code70518-2032-0
Package Description30 TABLET in 1 BLISTER PACK (70518-2032-0)
Product NDC70518-2032
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameAcyclovir
Non-Proprietary NameAcyclovir
Dosage FormTABLET
UsageORAL
Start Marketing Date20190419
Marketing Category NameANDA
Application NumberANDA210401
ManufacturerREMEDYREPACK INC.
Substance NameACYCLOVIR
Strength800
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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