acyclovir (Zydus Pharmaceuticals (USA) Inc.)


Welcome to the PulseAid listing for the acyclovir drug offered from Zydus Pharmaceuticals (USA) Inc.. 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: Zydus Pharmaceuticals (USA) Inc.
NON-PROPRIETARY NAME: ACYCLOVIR
SUBSTANCE NAME: ACYCLOVIR SODIUM
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: INTRAVENOUS
DOSAGE FORM: INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION
MARKETING CATEGORY NAME: ANDA
START MARKETING DATE: 2017-08-17
END MARKETING DATE: 0000-00-00


acyclovir HUMAN PRESCRIPTION DRUG Details:

Item Descriptionacyclovir from Zydus Pharmaceuticals (USA) Inc.
LABELER NAME: Zydus Pharmaceuticals (USA) Inc.
DEA SCHEDULE:
ACTIVE STRENGTH: 500(mg/1)
START MARKETING DATE: 2017-08-17
END MARKETING DATE: 0000-00-00
PRODUCT ID: 68382-125_c533d735-f4c5-4c7d-8fa4-64ede71ec261
PRODUCT NDC: 68382-125
APPLICATION NUMBER: ANDA206606

Other ACYCLOVIR SODIUM Pharmaceutical Manufacturers / Labelers:

Manufacturer / LabelerProprietary Name
APP Pharmaceuticals, LLCAcyclovir
AuroMedics Pharma LLCAcyclovir Sodium
Cadila Healthcare Limitedacyclovir
Fresenius Kabi USA, LLCAcyclovir
West-Ward Pharmaceuticals CorpAcyclovir
Zydus Pharmaceuticals (USA) Inc.acyclovir