| NDC Code | 53808-0635-1 |
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| Package Description | 30 TABLET, FILM COATED in 1 BLISTER PACK (53808-0635-1) |
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| Product NDC | 53808-0635 |
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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 | 20130101 |
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| Marketing Category Name | ANDA |
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| Application Number | ANDA077655 |
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| Manufacturer | State of Florida DOH Central Pharmacy |
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| Substance Name | VALACYCLOVIR HYDROCHLORIDE |
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| Strength | 500 |
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| Strength Unit | mg/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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