Nutmeg - 36987-1710-4 - (Nutmeg)

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Drug Information of Nutmeg

Product NDC: 36987-1710
Proprietary Name: Nutmeg
Non Proprietary Name: Nutmeg
Active Ingredient(s): .05    g/mL & nbsp;   Nutmeg
Administration Route(s): INTRADERMAL; SUBCUTANEOUS
Dosage Form(s): INJECTION, SOLUTION
Coding System: National Drug Codes(NDC)

Labeler Information of Nutmeg

Product NDC: 36987-1710
Labeler Name: Nelco Laboratories, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: BLA102192
Marketing Category: BLA
Start Marketing Date: 19720829

Package Information of Nutmeg

Package NDC: 36987-1710-4
Package Description: 50 mL in 1 VIAL, MULTI-DOSE (36987-1710-4)

NDC Information of Nutmeg

NDC Code 36987-1710-4
Proprietary Name Nutmeg
Package Description 50 mL in 1 VIAL, MULTI-DOSE (36987-1710-4)
Product NDC 36987-1710
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Nutmeg
Dosage Form Name INJECTION, SOLUTION
Route Name INTRADERMAL; SUBCUTANEOUS
Start Marketing Date 19720829
Marketing Category Name BLA
Labeler Name Nelco Laboratories, Inc.
Substance Name NUTMEG
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],Plant Proteins [Chemical/Ingredient],Dietary Proteins [Chemical/Ingredient],Food Additives [Chemical/Ingredient],Seed Storage Proteins [Chemical/Ingredient]

Complete Information of Nutmeg


General Information