| NDC Code | 21695-832-10 |
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| Package Description | 10 TABLET, FILM COATED in 1 BOTTLE (21695-832-10) |
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| Product NDC | 21695-832 |
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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 | 20091203 |
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| Marketing Category Name | ANDA |
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| Application Number | ANDA077135 |
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| Manufacturer | Rebel Distributors Corp |
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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 | Herpes Zoster Virus Nucleoside Analog DNA Polymerase Inhibitor [EPC],Herpesvirus Nucleoside Analog DNA Polymerase Inhibitor [EPC],Nucleoside Analog [EXT],Herpes Simplex Virus Nucleoside Analog DNA Polymerase Inhibitor [EPC],DNA Polymerase Inhibitors [MoA] |
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