SPEARMINT - 54575-459-10 - (spearmint)

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Drug Information of SPEARMINT

Product NDC: 54575-459
Proprietary Name: SPEARMINT
Non Proprietary Name: spearmint
Active Ingredient(s): 1    g/20mL & nbsp;   spearmint
Administration Route(s): PERCUTANEOUS; SUBCUTANEOUS
Dosage Form(s): INJECTION, SOLUTION
Coding System: National Drug Codes(NDC)

Labeler Information of SPEARMINT

Product NDC: 54575-459
Labeler Name: Allergy Laboratories, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: BLA102192
Marketing Category: BLA
Start Marketing Date: 19720829

Package Information of SPEARMINT

Package NDC: 54575-459-10
Package Description: 10 mL in 1 VIAL, MULTI-DOSE (54575-459-10)

NDC Information of SPEARMINT

NDC Code 54575-459-10
Proprietary Name SPEARMINT
Package Description 10 mL in 1 VIAL, MULTI-DOSE (54575-459-10)
Product NDC 54575-459
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name spearmint
Dosage Form Name INJECTION, SOLUTION
Route Name PERCUTANEOUS; SUBCUTANEOUS
Start Marketing Date 19720829
Marketing Category Name BLA
Labeler Name Allergy Laboratories, Inc.
Substance Name SPEARMINT
Strength Number 1
Strength Unit g/20mL
Pharmaceutical Classes Non-Standardized Food Allergenic Extract [EPC],Increased Histamine Release [PE],Cell-mediated Immunity [PE],Food Additives [Chemical/Ingredient],Allergens [Chemical/Ingredient],Dietary Proteins [Chemical/Ingredient]

Complete Information of SPEARMINT


General Information