"68788-7378-2" National Drug Code (NDC)

Acyclovir 21 TABLET in 1 BOTTLE (68788-7378-2)
(Preferred Pharmaceuticals Inc.)

NDC Code68788-7378-2
Package Description21 TABLET in 1 BOTTLE (68788-7378-2)
Product NDC68788-7378
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameAcyclovir
Non-Proprietary NameAcyclovir
Dosage FormTABLET
UsageORAL
Start Marketing Date20160825
Marketing Category NameANDA
Application NumberANDA204314
ManufacturerPreferred Pharmaceuticals Inc.
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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