STRAWBERRY - 0268-6220-06 - (Strawberry)

Alphabetical Index


Drug Information of STRAWBERRY

Product NDC: 0268-6220
Proprietary Name: STRAWBERRY
Non Proprietary Name: Strawberry
Active Ingredient(s): .1    g/mL & nbsp;   Strawberry
Administration Route(s): PERCUTANEOUS
Dosage Form(s): INJECTION, SOLUTION
Coding System: National Drug Codes(NDC)

Labeler Information of STRAWBERRY

Product NDC: 0268-6220
Labeler Name: ALK-Abello, Inc.
Product Type: NON-STANDARDIZED ALLERGENIC
FDA Application Number: BLA103753
Marketing Category: BLA
Start Marketing Date: 19650101

Package Information of STRAWBERRY

Package NDC: 0268-6220-06
Package Description: 5 mL in 1 VIAL, MULTI-DOSE (0268-6220-06)

NDC Information of STRAWBERRY

NDC Code 0268-6220-06
Proprietary Name STRAWBERRY
Package Description 5 mL in 1 VIAL, MULTI-DOSE (0268-6220-06)
Product NDC 0268-6220
Product Type Name NON-STANDARDIZED ALLERGENIC
Non Proprietary Name Strawberry
Dosage Form Name INJECTION, SOLUTION
Route Name PERCUTANEOUS
Start Marketing Date 19650101
Marketing Category Name BLA
Labeler Name ALK-Abello, Inc.
Substance Name STRAWBERRY
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 STRAWBERRY


General Information