"53002-0084-3" National Drug Code (NDC)

Acyclovir 21 TABLET in 1 BOTTLE (53002-0084-3)
(RPK Pharmaceuticals, Inc.)

NDC Code53002-0084-3
Package Description21 TABLET in 1 BOTTLE (53002-0084-3)
Product NDC53002-0084
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameAcyclovir
Non-Proprietary NameAcyclovir
Dosage FormTABLET
UsageORAL
Start Marketing Date20200815
Marketing Category NameANDA
Application NumberANDA209366
ManufacturerRPK Pharmaceuticals, 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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