"72189-232-30" National Drug Code (NDC)

Acyclovir 30 TABLET in 1 BOTTLE (72189-232-30)
(DIRECT RX)

NDC Code72189-232-30
Package Description30 TABLET in 1 BOTTLE (72189-232-30)
Product NDC72189-232
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameAcyclovir
Non-Proprietary NameAcyclovir
Dosage FormTABLET
UsageORAL
Start Marketing Date20210913
Marketing Category NameANDA
Application NumberANDA075382
ManufacturerDIRECT RX
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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