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VALTREX
VALTREX - 0173-0933-56 - (valacyclovir hydrochloride)
Drug Information of VALTREX
| Product NDC: | 0173-0933 |
| Proprietary Name: | VALTREX |
| Non Proprietary Name: | valacyclovir hydrochloride |
| Active Ingredient(s): | 500 mg/1 & nbsp; valacyclovir hydrochloride |
| Administration Route(s): | ORAL |
| Dosage Form(s): | TABLET, FILM COATED |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of VALTREX
| Product NDC: | 0173-0933 |
| Labeler Name: | GlaxoSmithKline LLC |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | NDA020487 |
| Marketing Category: | NDA |
| Start Marketing Date: | 19950801 |
Package Information of VALTREX
| Package NDC: | 0173-0933-56 |
| Package Description: | 100 TABLET, FILM COATED in 1 BOX, UNIT-DOSE (0173-0933-56) |
NDC Information of VALTREX
| NDC Code | 0173-0933-56 |
| Proprietary Name | VALTREX |
| Package Description | 100 TABLET, FILM COATED in 1 BOX, UNIT-DOSE (0173-0933-56) |
| Product NDC | 0173-0933 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | valacyclovir hydrochloride |
| Dosage Form Name | TABLET, FILM COATED |
| Route Name | ORAL |
| Start Marketing Date | 19950801 |
| Marketing Category Name | NDA |
| Labeler Name | GlaxoSmithKline LLC |
| Substance Name | VALACYCLOVIR HYDROCHLORIDE |
| Strength Number | 500 |
| Strength Unit | mg/1 |
| Pharmaceutical 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 [Chemical/Ingredient] |
