Daunorubicin Hydrochloride (Halison Pharmaceuiticals USA, Inc)


Welcome to the PulseAid listing for the Daunorubicin Hydrochloride drug offered from Halison Pharmaceuiticals USA, Inc. This Anthracycline Topoisomerase Inhibitor [EPC],Anthracyclines [Chemical/Ingredient],Topoisomerase Inhibitors [MoA] 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: Halison Pharmaceuiticals USA, Inc
NON-PROPRIETARY NAME: daunorubicin hydrochloride
SUBSTANCE NAME: DAUNORUBICIN HYDROCHLORIDE
TYPE: HUMAN PRESCRIPTION DRUG
PHARMA CLASS: Anthracycline Topoisomerase Inhibitor [EPC],Anthracyclines [Chemical/Ingredient],Topoisomerase Inhibitors [MoA]
ROUTE: INTRAVENOUS
DOSAGE FORM: INJECTION, POWDER, FOR SOLUTION
MARKETING CATEGORY NAME: UNAPPROVED DRUG OTHER
START MARKETING DATE: 2016-10-01
END MARKETING DATE: 0000-00-00


Daunorubicin Hydrochloride HUMAN PRESCRIPTION DRUG Details:

Item DescriptionDaunorubicin Hydrochloride from Halison Pharmaceuiticals USA, Inc
LABELER NAME: Halison Pharmaceuiticals USA, Inc
DEA SCHEDULE:
ACTIVE STRENGTH: 20(mg/4mL)
START MARKETING DATE: 2016-10-01
END MARKETING DATE: 0000-00-00
PRODUCT ID: 42658-007_6a7ddc81-d6b3-420c-911a-17d0d9a6229a
PRODUCT NDC: 42658-007
APPLICATION NUMBER:

Other DAUNORUBICIN HYDROCHLORIDE Pharmaceutical Manufacturers / Labelers:

Manufacturer / LabelerProprietary Name
Halison Pharmaceuiticals USA, IncDaunorubicin Hydrochloride
Teva Parenteral Medicines, Inc.daunorubicin hydrochloride