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: | INTRAMUSCULAR; INTRAVENOUS; SUBCUTANEOUS |
| DOSAGE FORM: | INJECTION |
| MARKETING CATEGORY NAME: | UNAPPROVED DRUG OTHER |
| START MARKETING DATE: | 2009-04-01 |
| 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: |
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| ACTIVE STRENGTH: | 50(mg/mL) |
| START MARKETING DATE: | 2009-04-01 |
| END MARKETING DATE: | 0000-00-00 |
| PRODUCT ID: | 17478-515_c6d186e1-72f1-44e3-ae53-a45df5bf8f59 |
| PRODUCT NDC: | 17478-515 |
| APPLICATION NUMBER: | |
Other EPHEDRINE SULFATE Pharmaceutical Manufacturers / Labelers:
