POPPY SEED - 54575-442-10 - (poppy seed)

Alphabetical Index


Drug Information of POPPY SEED

Product NDC: 54575-442
Proprietary Name: POPPY SEED
Non Proprietary Name: poppy seed
Active Ingredient(s): 1    g/20mL & nbsp;   poppy seed
Administration Route(s): PERCUTANEOUS; SUBCUTANEOUS
Dosage Form(s): INJECTION, SOLUTION
Coding System: National Drug Codes(NDC)

Labeler Information of POPPY SEED

Product NDC: 54575-442
Labeler Name: Allergy Laboratories, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: BLA102192
Marketing Category: BLA
Start Marketing Date: 19720829

Package Information of POPPY SEED

Package NDC: 54575-442-10
Package Description: 10 mL in 1 VIAL, MULTI-DOSE (54575-442-10)

NDC Information of POPPY SEED

NDC Code 54575-442-10
Proprietary Name POPPY SEED
Package Description 10 mL in 1 VIAL, MULTI-DOSE (54575-442-10)
Product NDC 54575-442
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name poppy 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 POPPY SEED
Strength Number 1
Strength Unit g/20mL
Pharmaceutical Classes Non-Standardized Plant Allergenic Extract [EPC],Non-Standardized Food Allergenic Extract [EPC],Increased Histamine Release [PE],Cell-mediated Immunity [PE],Allergens [Chemical/Ingredient],Dietary Proteins [Chemical/Ingredient],Plant Proteins [Chemical/Ingredient],Seed Storage Proteins [Chemical/Ingredient]

Complete Information of POPPY SEED


General Information