| NDC Code | 65862-753-99 |
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| Package Description | 1000 TABLET in 1 BOTTLE (65862-753-99) |
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| Product NDC | 65862-753 |
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| Product Type Name | HUMAN PRESCRIPTION DRUG |
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| Proprietary Name | Valganciclovir Hydrochloride |
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| Non-Proprietary Name | Valganciclovir Hydrochloride |
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| Dosage Form | TABLET |
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| Usage | ORAL |
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| Start Marketing Date | 20160331 |
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| Marketing Category Name | ANDA |
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| Application Number | ANDA204750 |
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| Manufacturer | Aurobindo Pharma Limited |
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| Substance Name | VALGANCICLOVIR HYDROCHLORIDE |
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| Strength | 450 |
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| Strength Unit | mg/1 |
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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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