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Valacyclovir hydrochloride
Valacyclovir hydrochloride - 49349-886-03 - (Valacyclovir hydrochloride)
Drug Information of Valacyclovir hydrochloride
| Product NDC: | 49349-886 |
| Proprietary Name: | Valacyclovir hydrochloride |
| Non Proprietary Name: | Valacyclovir hydrochloride |
| Active Ingredient(s): | 1 g/1 & nbsp; Valacyclovir hydrochloride |
| Administration Route(s): | ORAL |
| Dosage Form(s): | TABLET, FILM COATED |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Valacyclovir hydrochloride
| Product NDC: | 49349-886 |
| Labeler Name: | REMEDYREPACK INC. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA090370 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20130409 |
Package Information of Valacyclovir hydrochloride
| Package NDC: | 49349-886-03 |
| Package Description: | 20 TABLET, FILM COATED in 1 VIAL (49349-886-03) |
NDC Information of Valacyclovir hydrochloride
| NDC Code | 49349-886-03 |
| Proprietary Name | Valacyclovir hydrochloride |
| Package Description | 20 TABLET, FILM COATED in 1 VIAL (49349-886-03) |
| Product NDC | 49349-886 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Valacyclovir hydrochloride |
| Dosage Form Name | TABLET, FILM COATED |
| Route Name | ORAL |
| Start Marketing Date | 20130409 |
| Marketing Category Name | ANDA |
| Labeler Name | REMEDYREPACK INC. |
| Substance Name | VALACYCLOVIR HYDROCHLORIDE |
| Strength Number | 1 |
| Strength Unit | g/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] |
