Ephedrine Sulfate (Akorn, Inc.)
Welcome to the PulseAid listing for the Ephedrine Sulfate drug offered from Akorn, Inc.. This alpha-Adrenergic Agonist [EPC],Adrenergic alpha-Agonists [MoA],beta-Adrenergic Agonist [EPC],Adrenergic beta-Agonists [MoA],Norepinephrine Releasing Agent [EPC],Increased Norepinephrine Activity [PE] 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: | Akorn, Inc. |
NON-PROPRIETARY NAME: | Ephedrine Sulfate |
SUBSTANCE NAME: | EPHEDRINE SULFATE |
TYPE: | HUMAN PRESCRIPTION DRUG |
PHARMA CLASS: | alpha-Adrenergic Agonist [EPC],Adrenergic alpha-Agonists [MoA],beta-Adrenergic Agonist [EPC],Adrenergic beta-Agonists [MoA],Norepinephrine Releasing Agent [EPC],Increased Norepinephrine Activity [PE] |
ROUTE: | INTRAVENOUS |
DOSAGE FORM: | INJECTION |
MARKETING CATEGORY NAME: | NDA |
START MARKETING DATE: | 2017-03-01 |
END MARKETING DATE: | 0000-00-00 |
Ephedrine Sulfate HUMAN PRESCRIPTION DRUG Details:
Item Description | Ephedrine Sulfate from Akorn, Inc. |
LABELER NAME: | Akorn, Inc. |
DEA SCHEDULE: |
|
ACTIVE STRENGTH: | 50(mg/mL) |
START MARKETING DATE: | 2017-03-01 |
END MARKETING DATE: | 0000-00-00 |
PRODUCT ID: | 17478-415_bc28112f-19e3-4f31-b8a0-13fdc8944680 |
PRODUCT NDC: | 17478-415 |
APPLICATION NUMBER: | NDA208609 |
Other EPHEDRINE SULFATE Pharmaceutical Manufacturers / Labelers: