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Brussels Sprout - 36987-1420-1 - (Brussels Sprout)

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Drug Information of Brussels Sprout

Product NDC: 36987-1420
Proprietary Name: Brussels Sprout
Non Proprietary Name: Brussels Sprout
Active Ingredient(s): .1    g/mL & nbsp;   Brussels Sprout
Administration Route(s): INTRADERMAL; SUBCUTANEOUS
Dosage Form(s): INJECTION, SOLUTION
Coding System: National Drug Codes(NDC)

Labeler Information of Brussels Sprout

Product NDC: 36987-1420
Labeler Name: Nelco Laboratories, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: BLA102192
Marketing Category: BLA
Start Marketing Date: 19720829

Package Information of Brussels Sprout

Package NDC: 36987-1420-1
Package Description: 5 mL in 1 VIAL, MULTI-DOSE (36987-1420-1)

NDC Information of Brussels Sprout

NDC Code 36987-1420-1
Proprietary Name Brussels Sprout
Package Description 5 mL in 1 VIAL, MULTI-DOSE (36987-1420-1)
Product NDC 36987-1420
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Brussels Sprout
Dosage Form Name INJECTION, SOLUTION
Route Name INTRADERMAL; SUBCUTANEOUS
Start Marketing Date 19720829
Marketing Category Name BLA
Labeler Name Nelco Laboratories, Inc.
Substance Name BRUSSELS SPROUT
Strength Number .1
Strength Unit g/mL
Pharmaceutical Classes Non-Standardized Plant Allergenic Extract [EPC],Non-Standardized Food Allergenic Extract [EPC],Increased Histamine Release [PE],Cell-mediated Immunity [PE],Allergens [Chemical/Ingredient],Dietary Proteins [Chemical/Ingredient],Plant Proteins [Chemical/Ingredient],Vegetable Proteins [Chemical/Ingredient]

Complete Information of Brussels Sprout


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