Orris Root - 36987-2235-1 - (Orris Root)

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Drug Information of Orris Root

Product NDC: 36987-2235
Proprietary Name: Orris Root
Non Proprietary Name: Orris Root
Active Ingredient(s): .05    g/mL & nbsp;   Orris Root
Administration Route(s): INTRADERMAL; SUBCUTANEOUS
Dosage Form(s): INJECTION, SOLUTION
Coding System: National Drug Codes(NDC)

Labeler Information of Orris Root

Product NDC: 36987-2235
Labeler Name: Nelco Laboratories, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: BLA102192
Marketing Category: BLA
Start Marketing Date: 19720829

Package Information of Orris Root

Package NDC: 36987-2235-1
Package Description: 5 mL in 1 VIAL, MULTI-DOSE (36987-2235-1)

NDC Information of Orris Root

NDC Code 36987-2235-1
Proprietary Name Orris Root
Package Description 5 mL in 1 VIAL, MULTI-DOSE (36987-2235-1)
Product NDC 36987-2235
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Orris Root
Dosage Form Name INJECTION, SOLUTION
Route Name INTRADERMAL; SUBCUTANEOUS
Start Marketing Date 19720829
Marketing Category Name BLA
Labeler Name Nelco Laboratories, Inc.
Substance Name IRIS GERMANICA VAR. FLORENTINA ROOT
Strength Number .05
Strength Unit g/mL
Pharmaceutical Classes 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]

Complete Information of Orris Root


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