"71335-1077-2" National Drug Code (NDC)

Acyclovir 28 TABLET in 1 BOTTLE (71335-1077-2)
(Bryant Ranch Prepack)

NDC Code71335-1077-2
Package Description28 TABLET in 1 BOTTLE (71335-1077-2)
Product NDC71335-1077
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameAcyclovir
Non-Proprietary NameAcyclovir
Dosage FormTABLET
UsageORAL
Start Marketing Date20180504
Marketing Category NameANDA
Application NumberANDA210401
ManufacturerBryant Ranch Prepack
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]

Find more : http://www.hipaaspace.com/medical_billing/coding/national.drug.codes/71335-1077-2