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BLACKEYED PEA - 54575-430-50 - (black-eyed pea)

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Drug Information of BLACKEYED PEA

Product NDC: 54575-430
Proprietary Name: BLACKEYED PEA
Non Proprietary Name: black-eyed pea
Active Ingredient(s): 1    g/20mL & nbsp;   black-eyed pea
Administration Route(s): PERCUTANEOUS; SUBCUTANEOUS
Dosage Form(s): INJECTION, SOLUTION
Coding System: National Drug Codes(NDC)

Labeler Information of BLACKEYED PEA

Product NDC: 54575-430
Labeler Name: Allergy Laboratories, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: BLA102192
Marketing Category: BLA
Start Marketing Date: 19720829

Package Information of BLACKEYED PEA

Package NDC: 54575-430-50
Package Description: 10 mL in 1 VIAL, MULTI-DOSE (54575-430-50)

NDC Information of BLACKEYED PEA

NDC Code 54575-430-50
Proprietary Name BLACKEYED PEA
Package Description 10 mL in 1 VIAL, MULTI-DOSE (54575-430-50)
Product NDC 54575-430
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name black-eyed pea
Dosage Form Name INJECTION, SOLUTION
Route Name PERCUTANEOUS; SUBCUTANEOUS
Start Marketing Date 19720829
Marketing Category Name BLA
Labeler Name Allergy Laboratories, Inc.
Substance Name BLACK-EYED PEA
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]

Complete Information of BLACKEYED PEA


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