IBANDRONATE SODIUM (Sun Pharmaceutical Industries Limited)
Welcome to the PulseAid listing for the IBANDRONATE SODIUM drug offered from Sun Pharmaceutical Industries Limited. 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: | Sun Pharmaceutical Industries Limited |
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: | 2014-02-15 |
END MARKETING DATE: | 0000-00-00 |
IBANDRONATE SODIUM HUMAN PRESCRIPTION DRUG Details:
Item Description | IBANDRONATE SODIUM from Sun Pharmaceutical Industries Limited |
LABELER NAME: | Sun Pharmaceutical Industries Limited |
DEA SCHEDULE: |
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ACTIVE STRENGTH: | 3(mg/3mL) |
START MARKETING DATE: | 2014-02-15 |
END MARKETING DATE: | 0000-00-00 |
PRODUCT ID: | 62756-218_35f7e448-c7e8-4e01-96db-c6e1af16339f |
PRODUCT NDC: | 62756-218 |
APPLICATION NUMBER: | ANDA090853 |
Other IBANDRONATE SODIUM Pharmaceutical Manufacturers / Labelers: