| NDC Code | 27241-159-19 |
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| Package Description | 1 POUCH in 1 CARTON (27241-159-19) > 1 BOTTLE in 1 POUCH > 100 mL in 1 BOTTLE |
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| Product NDC | 27241-159 |
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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 | POWDER, FOR SOLUTION |
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| Usage | ORAL |
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| Start Marketing Date | 20200113 |
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| Marketing Category Name | ANDA |
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| Application Number | ANDA212890 |
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| Manufacturer | Ajanta Pharma USA Inc. |
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| Substance Name | VALGANCICLOVIR HYDROCHLORIDE |
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| Strength | 50 |
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| Strength Unit | mg/mL |
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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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