| NDC Code | 68382-125-10 |
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| Package Description | 10 INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION in 1 CARTON (68382-125-10) |
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| Product NDC | 68382-125 |
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| Product Type Name | HUMAN PRESCRIPTION DRUG |
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| Proprietary Name | Acyclovir |
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| Non-Proprietary Name | Acyclovir |
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| Dosage Form | INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION |
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| Usage | INTRAVENOUS |
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| Start Marketing Date | 20170817 |
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| Marketing Category Name | ANDA |
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| Application Number | ANDA206606 |
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| Manufacturer | Zydus Pharmaceuticals USA Inc. |
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| Substance Name | ACYCLOVIR SODIUM |
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| Strength | 500 |
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| Strength Unit | mg/1 |
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| 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] |
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