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Horseradish - 36987-1698-3 - (Horseradish)

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Drug Information of Horseradish

Product NDC: 36987-1698
Proprietary Name: Horseradish
Non Proprietary Name: Horseradish
Active Ingredient(s): .05    g/mL & nbsp;   Horseradish
Administration Route(s): INTRADERMAL; SUBCUTANEOUS
Dosage Form(s): INJECTION, SOLUTION
Coding System: National Drug Codes(NDC)

Labeler Information of Horseradish

Product NDC: 36987-1698
Labeler Name: Nelco Laboratories, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: BLA102192
Marketing Category: BLA
Start Marketing Date: 19720829

Package Information of Horseradish

Package NDC: 36987-1698-3
Package Description: 30 mL in 1 VIAL, MULTI-DOSE (36987-1698-3)

NDC Information of Horseradish

NDC Code 36987-1698-3
Proprietary Name Horseradish
Package Description 30 mL in 1 VIAL, MULTI-DOSE (36987-1698-3)
Product NDC 36987-1698
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Horseradish
Dosage Form Name INJECTION, SOLUTION
Route Name INTRADERMAL; SUBCUTANEOUS
Start Marketing Date 19720829
Marketing Category Name BLA
Labeler Name Nelco Laboratories, Inc.
Substance Name HORSERADISH
Strength Number .05
Strength Unit g/mL
Pharmaceutical Classes Non-Standardized Food Allergenic Extract [EPC],Non-Standardized Plant Allergenic Extract [EPC],Increased Histamine Release [PE],Cell-mediated Immunity [PE],Allergens [Chemical/Ingredient],Dietary Proteins [Chemical/Ingredient],Plant Proteins [Chemical/Ingredient],Food Additives [Chemical/Ingredient]

Complete Information of Horseradish


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