| NDC Code | 63739-076-33 |
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| Package Description | 3 BLISTER PACK in 1 BOX, UNIT-DOSE (63739-076-33) / 10 TABLET, FILM COATED in 1 BLISTER PACK |
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| Product NDC | 63739-076 |
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| Product Type Name | HUMAN PRESCRIPTION DRUG |
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| Proprietary Name | Valganciclovir |
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| Non-Proprietary Name | Valganciclovir |
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| Dosage Form | TABLET, FILM COATED |
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| Usage | ORAL |
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| Start Marketing Date | 20220307 |
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| End Marketing Date | 20251130 |
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| Marketing Category Name | ANDA |
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| Application Number | ANDA205166 |
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| Manufacturer | McKesson Corporation DBA SKY Packaging |
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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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