Orris Root (Nelco Laboratories, Inc.)


Welcome to the PulseAid listing for the Orris Root drug offered from Nelco 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 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: Orris Root
SUBSTANCE NAME: IRIS GERMANICA VAR. FLORENTINA ROOT
TYPE: HUMAN PRESCRIPTION DRUG
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: INTRADERMAL; SUBCUTANEOUS
DOSAGE FORM: INJECTION, SOLUTION
MARKETING CATEGORY NAME: BLA
START MARKETING DATE: 1972-08-29
END MARKETING DATE: 0000-00-00


Orris Root HUMAN PRESCRIPTION DRUG Details:

Item DescriptionOrris Root from Nelco Laboratories, Inc.
LABELER NAME: Nelco Laboratories, Inc.
DEA SCHEDULE:
ACTIVE STRENGTH: 0.05(g/mL)
START MARKETING DATE: 1972-08-29
END MARKETING DATE: 0000-00-00
PRODUCT ID: 36987-2234_ec73bb3c-d08d-4a3b-92a9-d2bfd09da169
PRODUCT NDC: 36987-2234
APPLICATION NUMBER: BLA102192

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