Ephedrine Sulfate (Sandoz Inc)
Welcome to the PulseAid listing for the Ephedrine Sulfate drug offered from Sandoz 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: | Sandoz 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: | ANDA |
| START MARKETING DATE: | 2017-10-01 |
| END MARKETING DATE: | 0000-00-00 |
Ephedrine Sulfate HUMAN PRESCRIPTION DRUG Details:
| Item Description | Ephedrine Sulfate from Sandoz Inc |
| LABELER NAME: | Sandoz Inc |
| DEA SCHEDULE: |
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| ACTIVE STRENGTH: | 50(mg/mL) |
| START MARKETING DATE: | 2017-10-01 |
| END MARKETING DATE: | 0000-00-00 |
| PRODUCT ID: | 0781-3269_c8af7bb5-41da-4f8c-8acd-f489892a0d72 |
| PRODUCT NDC: | 0781-3269 |
| APPLICATION NUMBER: | ANDA209784 |
Other EPHEDRINE SULFATE Pharmaceutical Manufacturers / Labelers:
