Nutmeg - 36987-1712-2 - (Nutmeg)

Alphabetical Index


Drug Information of Nutmeg

Product NDC: 36987-1712
Proprietary Name: Nutmeg
Non Proprietary Name: Nutmeg
Active Ingredient(s): .1    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: 36987-1712
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: 36987-1712-2
Package Description: 10 mL in 1 VIAL, MULTI-DOSE (36987-1712-2)

NDC Information of Nutmeg

NDC Code 36987-1712-2
Proprietary Name Nutmeg
Package Description 10 mL in 1 VIAL, MULTI-DOSE (36987-1712-2)
Product NDC 36987-1712
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 .1
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