"70934-511-35" National Drug Code (NDC)

Acyclovir 35 TABLET in 1 BOTTLE, PLASTIC (70934-511-35)
(Denton Pharma, Inc. DBA Northwind Pharmaceuticals)

NDC Code70934-511-35
Package Description35 TABLET in 1 BOTTLE, PLASTIC (70934-511-35)
Product NDC70934-511
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameAcyclovir
Non-Proprietary NameAcyclovir
Dosage FormTABLET
UsageORAL
Start Marketing Date20200128
Marketing Category NameANDA
Application NumberANDA074891
ManufacturerDenton Pharma, Inc. DBA Northwind Pharmaceuticals
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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