| NDC Code | 55289-926-07 |
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| Package Description | 7 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (55289-926-07) |
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| Product NDC | 55289-926 |
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| Product Type Name | HUMAN PRESCRIPTION DRUG |
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| Proprietary Name | Valtrex |
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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 | 19950801 |
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| Marketing Category Name | NDA |
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| Application Number | NDA020487 |
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| Manufacturer | PD-Rx Pharmaceuticals, Inc. |
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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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