Ganciclovir (APP Pharmaceuticals, LLC)
Welcome to the PulseAid listing for the Ganciclovir drug offered from APP Pharmaceuticals, LLC. This Cytomegalovirus Nucleoside Analog DNA Polymerase Inhibitor [EPC],DNA Polymerase Inhibitors [MoA],Nucleoside Analog [Chemical/Ingredient],Nucleoside Analog Antiviral [EPC] 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: | APP Pharmaceuticals, LLC |
NON-PROPRIETARY NAME: | GANCICLOVIR SODIUM |
SUBSTANCE NAME: | GANCICLOVIR SODIUM |
TYPE: | HUMAN PRESCRIPTION DRUG |
PHARMA CLASS: | Cytomegalovirus Nucleoside Analog DNA Polymerase Inhibitor [EPC],DNA Polymerase Inhibitors [MoA],Nucleoside Analog [Chemical/Ingredient],Nucleoside Analog Antiviral [EPC] |
ROUTE: | INTRAVENOUS |
DOSAGE FORM: | INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION |
MARKETING CATEGORY NAME: | ANDA |
START MARKETING DATE: | 2010-06-28 |
END MARKETING DATE: | 0000-00-00 |
Ganciclovir HUMAN PRESCRIPTION DRUG Details:
Item Description | Ganciclovir from APP Pharmaceuticals, LLC |
LABELER NAME: | APP Pharmaceuticals, LLC |
DEA SCHEDULE: |
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ACTIVE STRENGTH: | 500(mg/10mL) |
START MARKETING DATE: | 2010-06-28 |
END MARKETING DATE: | 0000-00-00 |
PRODUCT ID: | 63323-315_dafaddc1-cf82-4ef8-922b-981380413d44 |
PRODUCT NDC: | 63323-315 |
APPLICATION NUMBER: | ANDA090658 |
Other GANCICLOVIR SODIUM Pharmaceutical Manufacturers / Labelers: