American Beech (Nelco Laboratories, Inc.)


Welcome to the PulseAid listing for the American Beech drug offered from Nelco 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 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: Nelco Laboratories, Inc.
NON-PROPRIETARY NAME: American Beech
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: INTRADERMAL; SUBCUTANEOUS
DOSAGE FORM: INJECTION, SOLUTION
MARKETING CATEGORY NAME: BLA
START MARKETING DATE: 1972-08-29
END MARKETING DATE: 0000-00-00


American Beech HUMAN PRESCRIPTION DRUG Details:

Item DescriptionAmerican Beech from Nelco Laboratories, Inc.
LABELER NAME: Nelco Laboratories, Inc.
DEA SCHEDULE:
ACTIVE STRENGTH: 10000([PNU]/mL)
START MARKETING DATE: 1972-08-29
END MARKETING DATE: 0000-00-00
PRODUCT ID: 36987-2517_0d62fd2a-d535-41ba-b17b-cf1e1f8b216b
PRODUCT NDC: 36987-2517
APPLICATION NUMBER: BLA102192

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