"70518-2518-1" National Drug Code (NDC)

Acyclovir 30 TABLET in 1 BLISTER PACK (70518-2518-1)
(REMEDYREPACK INC.)

NDC Code70518-2518-1
Package Description30 TABLET in 1 BLISTER PACK (70518-2518-1)
Product NDC70518-2518
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameAcyclovir
Non-Proprietary NameAcyclovir
Dosage FormTABLET
UsageORAL
Start Marketing Date20200101
Marketing Category NameANDA
Application NumberANDA203834
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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