ORRIS (ALK-Abello, Inc.)
Welcome to the PulseAid listing for the ORRIS drug offered from ALK-Abello, Inc.. This pharmaceutical is classified as a NON-STANDARDIZED ALLERGENIC. 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 NON-STANDARDIZED ALLERGENIC drug type category.
| LABELER NAME / MANUFACTURER: | ALK-Abello, Inc. |
| NON-PROPRIETARY NAME: | Orris Root |
| SUBSTANCE NAME: | ORRIS |
| TYPE: | NON-STANDARDIZED ALLERGENIC |
| PHARMA CLASS: | |
| ROUTE: | PERCUTANEOUS |
| DOSAGE FORM: | INJECTION, SOLUTION |
| MARKETING CATEGORY NAME: | BLA |
| START MARKETING DATE: | 1965-01-01 |
| END MARKETING DATE: | 0000-00-00 |
ORRIS NON-STANDARDIZED ALLERGENIC Details:
| Item Description | ORRIS from ALK-Abello, Inc. |
| LABELER NAME: | ALK-Abello, Inc. |
| DEA SCHEDULE: |
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| ACTIVE STRENGTH: | 0.05(g/mL) |
| START MARKETING DATE: | 1965-01-01 |
| END MARKETING DATE: | 0000-00-00 |
| PRODUCT ID: | 0268-6317_bb0f261e-93dd-41c4-90f8-95a5f603d8c3 |
| PRODUCT NDC: | 0268-6317 |
| APPLICATION NUMBER: | BLA103753 |
Other ORRIS Pharmaceutical Manufacturers / Labelers:
