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WHITE POTATO - 54575-445-50 - (potato)

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Drug Information of WHITE POTATO

Product NDC: 54575-445
Proprietary Name: WHITE POTATO
Non Proprietary Name: potato
Active Ingredient(s): 1    g/20mL & nbsp;   potato
Administration Route(s): PERCUTANEOUS; SUBCUTANEOUS
Dosage Form(s): INJECTION, SOLUTION
Coding System: National Drug Codes(NDC)

Labeler Information of WHITE POTATO

Product NDC: 54575-445
Labeler Name: Allergy Laboratories, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: BLA102192
Marketing Category: BLA
Start Marketing Date: 19720829

Package Information of WHITE POTATO

Package NDC: 54575-445-50
Package Description: 50 mL in 1 VIAL, MULTI-DOSE (54575-445-50)

NDC Information of WHITE POTATO

NDC Code 54575-445-50
Proprietary Name WHITE POTATO
Package Description 50 mL in 1 VIAL, MULTI-DOSE (54575-445-50)
Product NDC 54575-445
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name potato
Dosage Form Name INJECTION, SOLUTION
Route Name PERCUTANEOUS; SUBCUTANEOUS
Start Marketing Date 19720829
Marketing Category Name BLA
Labeler Name Allergy Laboratories, Inc.
Substance Name POTATO
Strength Number 1
Strength Unit g/20mL
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 WHITE POTATO


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