"49999-231-35" National Drug Code (NDC)

Acyclovir 35 TABLET in 1 BOTTLE (49999-231-35)
(Lake Erie Medical DBA Quality Care Products LLC)

NDC Code49999-231-35
Package Description35 TABLET in 1 BOTTLE (49999-231-35)
Product NDC49999-231
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameAcyclovir
Non-Proprietary NameAcyclovir
Dosage FormTABLET
UsageORAL
Start Marketing Date20060313
Marketing Category NameANDA
Application NumberANDA077309
ManufacturerLake Erie Medical DBA Quality Care Products LLC
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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