| NDC Code | 70518-3359-1 |
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| Package Description | 21 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70518-3359-1) |
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| Product NDC | 70518-3359 |
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| Product Type Name | HUMAN PRESCRIPTION DRUG |
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| Proprietary Name | Valacyclovir Hydrochloride |
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| Non-Proprietary Name | Valacyclovir Hydrochloride |
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| Dosage Form | TABLET, FILM COATED |
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| Usage | ORAL |
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| Start Marketing Date | 20220207 |
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| Marketing Category Name | ANDA |
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| Application Number | ANDA090682 |
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| Manufacturer | REMEDYREPACK INC. |
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| Substance Name | VALACYCLOVIR HYDROCHLORIDE |
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| Strength | 1 |
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| Strength Unit | g/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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