Orris Root (Allermed Laboratories, Inc.)


Welcome to the PulseAid listing for the Orris Root drug offered from Allermed Laboratories, Inc.. This Increased Histamine Release [PE],Cell-mediated Immunity [PE],Increased IgG Production [PE],Allergens [Chemical/Ingredient],Non-Standardized Plant Allergenic Extract [EPC],Plant Proteins [Chemical/Ingredient] 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: Allermed Laboratories, Inc.
NON-PROPRIETARY NAME: Orris Root
SUBSTANCE NAME: IRIS GERMANICA VAR. FLORENTINA ROOT
TYPE: NON-STANDARDIZED ALLERGENIC
PHARMA CLASS: Increased Histamine Release [PE],Cell-mediated Immunity [PE],Increased IgG Production [PE],Allergens [Chemical/Ingredient],Non-Standardized Plant Allergenic Extract [EPC],Plant Proteins [Chemical/Ingredient]
ROUTE: CUTANEOUS; INTRADERMAL; SUBCUTANEOUS
DOSAGE FORM: INJECTION
MARKETING CATEGORY NAME: BLA
START MARKETING DATE: 1974-03-12
END MARKETING DATE: 0000-00-00


Orris Root NON-STANDARDIZED ALLERGENIC Details:

Item DescriptionOrris Root from Allermed Laboratories, Inc.
LABELER NAME: Allermed Laboratories, Inc.
DEA SCHEDULE:
ACTIVE STRENGTH: 0.1(g/mL)
START MARKETING DATE: 1974-03-12
END MARKETING DATE: 0000-00-00
PRODUCT ID: 49643-020_4f1be4f6-9f9e-5c19-e054-00144ff8d46c
PRODUCT NDC: 49643-020
APPLICATION NUMBER: BLA102211

Other IRIS GERMANICA VAR. FLORENTINA ROOT Pharmaceutical Manufacturers / Labelers:

Manufacturer / LabelerProprietary Name
Allergy Laboratories, Inc.ORRIS ROOT
Allermed Laboratories, Inc.Orris Root
Antigen Laboratories, Inc.Orris Root
Nelco Laboratories, Inc.Orris Root