DMT SUIK (Asclemed USA, Inc.)
Welcome to the PulseAid listing for the DMT SUIK drug offered from Asclemed USA, Inc.. This Corticosteroid [EPC],Corticosteroid Hormone Receptor Agonists [MoA] 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: | Asclemed USA, Inc. |
| NON-PROPRIETARY NAME: | Dexamethasone Sodium Phosphate |
| SUBSTANCE NAME: | DEXAMETHASONE SODIUM PHOSPHATE |
| TYPE: | HUMAN PRESCRIPTION DRUG |
| PHARMA CLASS: | Corticosteroid [EPC],Corticosteroid Hormone Receptor Agonists [MoA] |
| ROUTE: | INTRAMUSCULAR; INTRAVENOUS |
| DOSAGE FORM: | INJECTION, SOLUTION |
| MARKETING CATEGORY NAME: | UNAPPROVED DRUG OTHER |
| START MARKETING DATE: | 2003-05-29 |
| END MARKETING DATE: | 0000-00-00 |
DMT SUIK HUMAN PRESCRIPTION DRUG Details:
| Item Description | DMT SUIK from Asclemed USA, Inc. |
| LABELER NAME: | Asclemed USA, Inc. |
| DEA SCHEDULE: |
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| ACTIVE STRENGTH: | 10(mg/mL) |
| START MARKETING DATE: | 2003-05-29 |
| END MARKETING DATE: | 0000-00-00 |
| PRODUCT ID: | 76420-270_17e4ecf6-8b51-4e46-8578-4ec2529d6d90 |
| PRODUCT NDC: | 76420-270 |
| APPLICATION NUMBER: | |
Other DEXAMETHASONE SODIUM PHOSPHATE Pharmaceutical Manufacturers / Labelers:
