POTATO - 0268-6206-06 - (White Potato)

Alphabetical Index


Drug Information of POTATO

Product NDC: 0268-6206
Proprietary Name: POTATO
Non Proprietary Name: White Potato
Active Ingredient(s): .1    g/mL & nbsp;   White Potato
Administration Route(s): PERCUTANEOUS
Dosage Form(s): INJECTION, SOLUTION
Coding System: National Drug Codes(NDC)

Labeler Information of POTATO

Product NDC: 0268-6206
Labeler Name: ALK-Abello, Inc.
Product Type: NON-STANDARDIZED ALLERGENIC
FDA Application Number: BLA103753
Marketing Category: BLA
Start Marketing Date: 19650101

Package Information of POTATO

Package NDC: 0268-6206-06
Package Description: 5 mL in 1 VIAL, MULTI-DOSE (0268-6206-06)

NDC Information of POTATO

NDC Code 0268-6206-06
Proprietary Name POTATO
Package Description 5 mL in 1 VIAL, MULTI-DOSE (0268-6206-06)
Product NDC 0268-6206
Product Type Name NON-STANDARDIZED ALLERGENIC
Non Proprietary Name White Potato
Dosage Form Name INJECTION, SOLUTION
Route Name PERCUTANEOUS
Start Marketing Date 19650101
Marketing Category Name BLA
Labeler Name ALK-Abello, Inc.
Substance Name POTATO
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 POTATO


General Information