PEA - 0268-6191-06 - (Green Pea English)

Alphabetical Index


Drug Information of PEA

Product NDC: 0268-6191
Proprietary Name: PEA
Non Proprietary Name: Green Pea English
Active Ingredient(s): .1    g/mL & nbsp;   Green Pea English
Administration Route(s): PERCUTANEOUS
Dosage Form(s): INJECTION, SOLUTION
Coding System: National Drug Codes(NDC)

Labeler Information of PEA

Product NDC: 0268-6191
Labeler Name: ALK-Abello, Inc.
Product Type: NON-STANDARDIZED ALLERGENIC
FDA Application Number: BLA103753
Marketing Category: BLA
Start Marketing Date: 19650101

Package Information of PEA

Package NDC: 0268-6191-06
Package Description: 5 mL in 1 VIAL, MULTI-DOSE (0268-6191-06)

NDC Information of PEA

NDC Code 0268-6191-06
Proprietary Name PEA
Package Description 5 mL in 1 VIAL, MULTI-DOSE (0268-6191-06)
Product NDC 0268-6191
Product Type Name NON-STANDARDIZED ALLERGENIC
Non Proprietary Name Green Pea English
Dosage Form Name INJECTION, SOLUTION
Route Name PERCUTANEOUS
Start Marketing Date 19650101
Marketing Category Name BLA
Labeler Name ALK-Abello, Inc.
Substance Name PEA
Strength Number .1
Strength Unit g/mL
Pharmaceutical Classes Non-Standardized Food Allergenic Extract [EPC],Increased Histamine Release [PE],Cell-mediated Immunity [PE],Allergens [Chemical/Ingredient],Dietary Proteins [Chemical/Ingredient],Vegetable Proteins [Chemical/Ingredient]

Complete Information of PEA


General Information