| NDC Code | 55111-552-42 |
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| Package Description | 42 TABLET, FILM COATED in 1 BOTTLE (55111-552-42) |
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| Product NDC | 55111-552 |
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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 | 20101206 |
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| Marketing Category Name | ANDA |
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| Application Number | ANDA079012 |
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| Manufacturer | Dr. Reddys Laboratories Limited |
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| Substance Name | VALACYCLOVIR |
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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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