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BARLEY MALT - 54575-410-50 - (barley malt)

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Drug Information of BARLEY MALT

Product NDC: 54575-410
Proprietary Name: BARLEY MALT
Non Proprietary Name: barley malt
Active Ingredient(s): 1    g/20mL & nbsp;   barley malt
Administration Route(s): PERCUTANEOUS; SUBCUTANEOUS
Dosage Form(s): INJECTION, SOLUTION
Coding System: National Drug Codes(NDC)

Labeler Information of BARLEY MALT

Product NDC: 54575-410
Labeler Name: Allergy Laboratories, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: BLA102192
Marketing Category: BLA
Start Marketing Date: 19720829

Package Information of BARLEY MALT

Package NDC: 54575-410-50
Package Description: 50 mL in 1 VIAL, MULTI-DOSE (54575-410-50)

NDC Information of BARLEY MALT

NDC Code 54575-410-50
Proprietary Name BARLEY MALT
Package Description 50 mL in 1 VIAL, MULTI-DOSE (54575-410-50)
Product NDC 54575-410
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name barley malt
Dosage Form Name INJECTION, SOLUTION
Route Name PERCUTANEOUS; SUBCUTANEOUS
Start Marketing Date 19720829
Marketing Category Name BLA
Labeler Name Allergy Laboratories, Inc.
Substance Name BARLEY MALT
Strength Number 1
Strength Unit g/20mL
Pharmaceutical Classes Non-Standardized Food Allergenic Extract [EPC],Non-Standardized Plant Allergenic Extract [EPC],Increased Histamine Release [PE],Cell-mediated Immunity [PE],Allergens [Chemical/Ingredient],Dietary Proteins [Chemical/Ingredient],Plant Proteins [Chemical/Ingredient],Grain Proteins [Chemical/Ingredient]

Complete Information of BARLEY MALT


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