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 DescriptionSORREL/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:

Manufacturer / LabelerProprietary Name
ALK-Abello, Inc.SORREL/DOCK MIX