Valacyclovir Hydrochloride (Dr. Reddys Laboratories Limited)


Welcome to the PulseAid listing for the Valacyclovir Hydrochloride drug offered from Dr. Reddys Laboratories Limited. This 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] pharmaceutical is classified as a HUMAN PRESCRIPTION DRUG. Below, you can view details for this drug, such as its dosage form, route of delivery, start market/end market dates, and more. We have also randomly listed additional pharmaceuticals used in the same HUMAN PRESCRIPTION DRUG drug type category.
LABELER NAME / MANUFACTURER: Dr. Reddys Laboratories Limited
NON-PROPRIETARY NAME: Valacyclovir Hydrochloride
SUBSTANCE NAME: VALACYCLOVIR
TYPE: HUMAN PRESCRIPTION DRUG
PHARMA CLASS: 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]
ROUTE: ORAL
DOSAGE FORM: TABLET, FILM COATED
MARKETING CATEGORY NAME: ANDA
START MARKETING DATE: 2010-12-06
END MARKETING DATE: 0000-00-00


Valacyclovir Hydrochloride HUMAN PRESCRIPTION DRUG Details:

Item DescriptionValacyclovir Hydrochloride from Dr. Reddys Laboratories Limited
LABELER NAME: Dr. Reddys Laboratories Limited
DEA SCHEDULE:
ACTIVE STRENGTH: 500(mg/1)
START MARKETING DATE: 2010-12-06
END MARKETING DATE: 0000-00-00
PRODUCT ID: 55111-552_8d4b0d73-3618-171b-e90a-fdeeeded3810
PRODUCT NDC: 55111-552
APPLICATION NUMBER: ANDA079012

Other VALACYCLOVIR Pharmaceutical Manufacturers / Labelers:

Manufacturer / LabelerProprietary Name
Dr. Reddys Laboratories LimitedValacyclovir Hydrochloride