DOXOrubicin Hydrochloride (Sun Pharmaceutical Industries Limited)
Welcome to the PulseAid listing for the DOXOrubicin Hydrochloride drug offered from Sun Pharmaceutical Industries Limited. 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: | Sun Pharmaceutical Industries Limited |
NON-PROPRIETARY NAME: | DOXOrubicin Hydrochloride |
SUBSTANCE NAME: | DOXORUBICIN HYDROCHLORIDE |
TYPE: | HUMAN PRESCRIPTION DRUG |
PHARMA CLASS: | Anthracycline Topoisomerase Inhibitor [EPC],Anthracyclines [Chemical/Ingredient],Topoisomerase Inhibitors [MoA] |
ROUTE: | INTRAVENOUS |
DOSAGE FORM: | INJECTION, SOLUTION |
MARKETING CATEGORY NAME: | ANDA |
START MARKETING DATE: | 2012-02-20 |
END MARKETING DATE: | 0000-00-00 |
DOXOrubicin Hydrochloride HUMAN PRESCRIPTION DRUG Details:
Item Description | DOXOrubicin Hydrochloride from Sun Pharmaceutical Industries Limited |
LABELER NAME: | Sun Pharmaceutical Industries Limited |
DEA SCHEDULE: |
|
ACTIVE STRENGTH: | 2(mg/mL) |
START MARKETING DATE: | 2012-02-20 |
END MARKETING DATE: | 0000-00-00 |
PRODUCT ID: | 62756-826_90644999-157b-40d5-8307-e8caf8a885a2 |
PRODUCT NDC: | 62756-826 |
APPLICATION NUMBER: | ANDA091418 |
Other DOXORUBICIN HYDROCHLORIDE Pharmaceutical Manufacturers / Labelers: