| NDC Code | 51079-093-03 |
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| Package Description | 30 BLISTER PACK in 1 CARTON (51079-093-03) / 1 TABLET, FILM COATED in 1 BLISTER PACK (51079-093-01) |
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| Product NDC | 51079-093 |
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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 | 20110307 |
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| Marketing Category Name | ANDA |
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| Application Number | ANDA078518 |
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| Manufacturer | Mylan Institutional 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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