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SUNFLOWER SEED - 54575-463-50 - (sunflower seed)

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Drug Information of SUNFLOWER SEED

Product NDC: 54575-463
Proprietary Name: SUNFLOWER SEED
Non Proprietary Name: sunflower seed
Active Ingredient(s): 1    g/20mL & nbsp;   sunflower seed
Administration Route(s): PERCUTANEOUS; SUBCUTANEOUS
Dosage Form(s): INJECTION, SOLUTION
Coding System: National Drug Codes(NDC)

Labeler Information of SUNFLOWER SEED

Product NDC: 54575-463
Labeler Name: Allergy Laboratories, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: BLA102192
Marketing Category: BLA
Start Marketing Date: 19720829

Package Information of SUNFLOWER SEED

Package NDC: 54575-463-50
Package Description: 50 mL in 1 VIAL, MULTI-DOSE (54575-463-50)

NDC Information of SUNFLOWER SEED

NDC Code 54575-463-50
Proprietary Name SUNFLOWER SEED
Package Description 50 mL in 1 VIAL, MULTI-DOSE (54575-463-50)
Product NDC 54575-463
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name sunflower seed
Dosage Form Name INJECTION, SOLUTION
Route Name PERCUTANEOUS; SUBCUTANEOUS
Start Marketing Date 19720829
Marketing Category Name BLA
Labeler Name Allergy Laboratories, Inc.
Substance Name SUNFLOWER SEED
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],Seed Storage Proteins [Chemical/Ingredient],Plant Proteins [Chemical/Ingredient]

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