risedronate sodium (Sun Pharma Global FZE)


Welcome to the PulseAid listing for the risedronate sodium drug offered from Sun Pharma Global FZE. 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 Pharma Global FZE
NON-PROPRIETARY NAME: risedronate sodium
SUBSTANCE NAME: RISEDRONATE SODIUM HEMI-PENTAHYDRATE
TYPE: HUMAN PRESCRIPTION DRUG
PHARMA CLASS: Bisphosphonate [EPC],Diphosphonates [Chemical/Ingredient]
ROUTE: ORAL
DOSAGE FORM: TABLET, FILM COATED
MARKETING CATEGORY NAME: ANDA
START MARKETING DATE: 2015-11-30
END MARKETING DATE: 0000-00-00


risedronate sodium HUMAN PRESCRIPTION DRUG Details:

Item Descriptionrisedronate sodium from Sun Pharma Global FZE
LABELER NAME: Sun Pharma Global FZE
DEA SCHEDULE:
ACTIVE STRENGTH: 5(mg/1)
START MARKETING DATE: 2015-11-30
END MARKETING DATE: 0000-00-00
PRODUCT ID: 47335-666_22863a35-dfea-498d-9004-581769439767
PRODUCT NDC: 47335-666
APPLICATION NUMBER: ANDA090886

Other RISEDRONATE SODIUM HEMI-PENTAHYDRATE Pharmaceutical Manufacturers / Labelers:

Manufacturer / LabelerProprietary Name
Sun Pharma Global FZErisedronate sodium