| NDC Code | 70436-089-55 |
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| Package Description | 25 VIAL in 1 CARTON (70436-089-55) / 10 mL in 1 VIAL |
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| Product NDC | 70436-089 |
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| Product Type Name | HUMAN PRESCRIPTION DRUG |
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| Proprietary Name | Ganciclovir |
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| Non-Proprietary Name | Ganciclovir Sodium |
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| Dosage Form | INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION |
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| Usage | INTRAVENOUS |
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| Start Marketing Date | 20190101 |
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| Marketing Category Name | ANDA |
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| Application Number | ANDA204204 |
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| Manufacturer | Slate Run Pharmaceuticals, LLC |
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| Substance Name | GANCICLOVIR SODIUM |
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| Strength | 500 |
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| Strength Unit | mg/10mL |
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| Pharmacy Classes | Cytomegalovirus Nucleoside Analog DNA Polymerase Inhibitor [EPC], DNA Polymerase Inhibitors [MoA], Nucleoside Analog Antiviral [EPC], Nucleoside Analog [EXT] |
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