SORREL/DOCK MIX (ALK-Abello, Inc.)
Welcome to the PulseAid listing for the SORREL/DOCK MIX 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: | RUMEX ACETOSELLA and RUMEX CRISPUS |
SUBSTANCE NAME: | RUMEX ACETOSELLA WHOLE; RUMEX CRISPUS TOP |
TYPE: | NON-STANDARDIZED ALLERGENIC |
PHARMA CLASS: | |
ROUTE: | PERCUTANEOUS; SUBCUTANEOUS |
DOSAGE FORM: | INJECTION, SOLUTION |
MARKETING CATEGORY NAME: | BLA |
START MARKETING DATE: | 1965-01-01 |
END MARKETING DATE: | 0000-00-00 |
SORREL/DOCK MIX NON-STANDARDIZED ALLERGENIC Details:
Item Description | SORREL/DOCK MIX from ALK-Abello, Inc. |
LABELER NAME: | ALK-Abello, Inc. |
DEA SCHEDULE: |
|
ACTIVE STRENGTH: | .05; .05(g/mL; g/mL) |
START MARKETING DATE: | 1965-01-01 |
END MARKETING DATE: | 0000-00-00 |
PRODUCT ID: | 0268-1302_356d3b28-7f35-4b8d-965e-dc8fc14856f3 |
PRODUCT NDC: | 0268-1302 |
APPLICATION NUMBER: | BLA103753 |
Other RUMEX ACETOSELLA WHOLE; RUMEX CRISPUS TOP Pharmaceutical Manufacturers / Labelers: