ISOXSUPRINE HYDROCHLORIDE (ECI Pharmaceuticals LLC)


Welcome to the PulseAid listing for the ISOXSUPRINE HYDROCHLORIDE drug offered from ECI Pharmaceuticals LLC. This 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: ECI Pharmaceuticals LLC
NON-PROPRIETARY NAME: isoxsuprine hydrochloride
SUBSTANCE NAME: ISOXSUPRINE HYDROCHLORIDE
TYPE: HUMAN PRESCRIPTION DRUG
PHARMA CLASS:
ROUTE: ORAL
DOSAGE FORM: TABLET
MARKETING CATEGORY NAME: UNAPPROVED DRUG OTHER
START MARKETING DATE: 2011-08-23
END MARKETING DATE: 0000-00-00


ISOXSUPRINE HYDROCHLORIDE HUMAN PRESCRIPTION DRUG Details:

Item DescriptionISOXSUPRINE HYDROCHLORIDE from ECI Pharmaceuticals LLC
LABELER NAME: ECI Pharmaceuticals LLC
DEA SCHEDULE:
ACTIVE STRENGTH: 20(mg/1)
START MARKETING DATE: 2011-08-23
END MARKETING DATE: 0000-00-00
PRODUCT ID: 51293-605_23eeca2c-6fb7-4f12-b18d-3c4ef3fb7419
PRODUCT NDC: 51293-605
APPLICATION NUMBER:

Other ISOXSUPRINE HYDROCHLORIDE Pharmaceutical Manufacturers / Labelers:

Manufacturer / LabelerProprietary Name
BI-COASTAL PHARMA INTERNATIONAL LIMITED LIABILITY COMPANYISOXSUPRINE HYDROCHLORIDE
Bi-Coastal Pharmaceutical CorporationISOXSUPRINE HYDROCHLORIDE
ECI Pharmaceuticals LLCISOXSUPRINE HYDROCHLORIDE
Vedco dba ValdarISOXSUPRINE HYDROCHLORIDE
Vista Pharmaceuticals, Inc.ISOXSUPRINE HYDROCHLORIDE