ORANGE - 0268-6187-06 - (Orange)

Alphabetical Index


Drug Information of ORANGE

Product NDC: 0268-6187
Proprietary Name: ORANGE
Non Proprietary Name: Orange
Active Ingredient(s): .1    g/mL & nbsp;   Orange
Administration Route(s): PERCUTANEOUS
Dosage Form(s): INJECTION, SOLUTION
Coding System: National Drug Codes(NDC)

Labeler Information of ORANGE

Product NDC: 0268-6187
Labeler Name: ALK-Abello, Inc.
Product Type: NON-STANDARDIZED ALLERGENIC
FDA Application Number: BLA103753
Marketing Category: BLA
Start Marketing Date: 19650101

Package Information of ORANGE

Package NDC: 0268-6187-06
Package Description: 5 mL in 1 VIAL, MULTI-DOSE (0268-6187-06)

NDC Information of ORANGE

NDC Code 0268-6187-06
Proprietary Name ORANGE
Package Description 5 mL in 1 VIAL, MULTI-DOSE (0268-6187-06)
Product NDC 0268-6187
Product Type Name NON-STANDARDIZED ALLERGENIC
Non Proprietary Name Orange
Dosage Form Name INJECTION, SOLUTION
Route Name PERCUTANEOUS
Start Marketing Date 19650101
Marketing Category Name BLA
Labeler Name ALK-Abello, Inc.
Substance Name ORANGE
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],Fruit Proteins [Chemical/Ingredient]

Complete Information of ORANGE


General Information