ibandronate sodium (Sagent Pharmaceuticals)
Welcome to the PulseAid listing for the ibandronate sodium drug offered from Sagent Pharmaceuticals. This Bisphosphonate [EPC],Diphosphonates [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: | Sagent Pharmaceuticals |
NON-PROPRIETARY NAME: | ibandronate sodium |
SUBSTANCE NAME: | IBANDRONATE SODIUM |
TYPE: | HUMAN PRESCRIPTION DRUG |
PHARMA CLASS: | Bisphosphonate [EPC],Diphosphonates [Chemical/Ingredient] |
ROUTE: | INTRAVENOUS |
DOSAGE FORM: | INJECTION, SOLUTION |
MARKETING CATEGORY NAME: | ANDA |
START MARKETING DATE: | 2014-09-02 |
END MARKETING DATE: | 0000-00-00 |
ibandronate sodium HUMAN PRESCRIPTION DRUG Details:
Item Description | ibandronate sodium from Sagent Pharmaceuticals |
LABELER NAME: | Sagent Pharmaceuticals |
DEA SCHEDULE: |
|
ACTIVE STRENGTH: | 3(mg/3mL) |
START MARKETING DATE: | 2014-09-02 |
END MARKETING DATE: | 0000-00-00 |
PRODUCT ID: | 25021-827_3af7be37-c284-47e8-a57a-9f61b7472445 |
PRODUCT NDC: | 25021-827 |
APPLICATION NUMBER: | ANDA202235 |
Other IBANDRONATE SODIUM Pharmaceutical Manufacturers / Labelers: