OYSTER (ALK-Abello, Inc.)


Welcome to the PulseAid listing for the OYSTER 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: EASTERN OYSTER
SUBSTANCE NAME: EASTERN OYSTER
TYPE: NON-STANDARDIZED ALLERGENIC
PHARMA CLASS:
ROUTE: PERCUTANEOUS
DOSAGE FORM: INJECTION, SOLUTION
MARKETING CATEGORY NAME: BLA
START MARKETING DATE: 1998-02-23
END MARKETING DATE: 0000-00-00


OYSTER NON-STANDARDIZED ALLERGENIC Details:

Item DescriptionOYSTER from ALK-Abello, Inc.
LABELER NAME: ALK-Abello, Inc.
DEA SCHEDULE:
ACTIVE STRENGTH: 0.1(mg/mL)
START MARKETING DATE: 1998-02-23
END MARKETING DATE: 0000-00-00
PRODUCT ID: 0268-6189_b5997c82-efde-4f24-b7d3-a2d65bb50997
PRODUCT NDC: 0268-6189
APPLICATION NUMBER: BLA103753

Other EASTERN OYSTER Pharmaceutical Manufacturers / Labelers:

Manufacturer / LabelerProprietary Name
ALK-Abello, Inc.OYSTER