"68382-049-10" National Drug Code (NDC)

NDC Code	68382-049-10
Package Description	10 VIAL, SINGLE-USE in 1 CARTON (68382-049-10) > 20 mL in 1 VIAL, SINGLE-USE (68382-049-01)
Product NDC	68382-049
Product Type Name	HUMAN PRESCRIPTION DRUG
Proprietary Name	Acyclovir
Non-Proprietary Name	Acyclovir
Dosage Form	INJECTION, SOLUTION
Usage	INTRAVENOUS
Start Marketing Date	20181127
Marketing Category Name	ANDA
Application Number	ANDA206535
Manufacturer	Zydus Pharmaceuticals (USA) Inc.
Substance Name	ACYCLOVIR SODIUM
Strength	50
Strength Unit	mg/mL
Pharmacy Classes	DNA 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]