AMERICAN BEECH POLLEN (Allergy Laboratories, Inc.)


Welcome to the PulseAid listing for the AMERICAN BEECH POLLEN drug offered from Allergy Laboratories, Inc.. This Non-Standardized Pollen Allergenic Extract [EPC],Increased Histamine Release [PE],Cell-mediated Immunity [PE],Increased IgG Production [PE],Pollen [Chemical/Ingredient],Allergens [Chemical/Ingredient] pharmaceutical is classified as a HUMAN PRESCRIPTION DRUG. Below, you can view the 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: Allergy Laboratories, Inc.
NON-PROPRIETARY NAME: fagus grandifolia pollen
SUBSTANCE NAME: FAGUS GRANDIFOLIA POLLEN
TYPE: HUMAN PRESCRIPTION DRUG
PHARMA CLASS: Non-Standardized Pollen Allergenic Extract [EPC],Increased Histamine Release [PE],Cell-mediated Immunity [PE],Increased IgG Production [PE],Pollen [Chemical/Ingredient],Allergens [Chemical/Ingredient]
ROUTE: PERCUTANEOUS; SUBCUTANEOUS
DOSAGE FORM: INJECTION, SOLUTION
MARKETING CATEGORY NAME: BLA
START MARKETING DATE: 1967-12-07
END MARKETING DATE: 0000-00-00


AMERICAN BEECH POLLEN HUMAN PRESCRIPTION DRUG Details:

Item DescriptionAMERICAN BEECH POLLEN from Allergy Laboratories, Inc.
LABELER NAME: Allergy Laboratories, Inc.
DEA SCHEDULE:
ACTIVE STRENGTH: 1(g/20mL)
START MARKETING DATE: 1967-12-07
END MARKETING DATE: 0000-00-00
PRODUCT ID: 54575-910_dbe7bebd-e445-4e59-8302-e706b795fbde
PRODUCT NDC: 54575-910
APPLICATION NUMBER: BLA101376

Other FAGUS GRANDIFOLIA POLLEN Pharmaceutical Manufacturers / Labelers:

Manufacturer / LabelerProprietary Name
ALK-Abello, Inc.CENTER-AL – FAGUS GRANDIFOLIA POLLEN
Allergy Laboratories, Inc.AMERICAN BEECH POLLEN
Allermed Laboratories, Inc.Beech Pollen
Antigen Laboratories, Inc.American Beech
Jubilant HollisterStier LLCPollens – Trees, Beech, American Fagus grandifolia
Nelco Laboratories, Inc.American Beech