BANANA - 54575-339-02 - (banana)

Alphabetical Index


Drug Information of BANANA

Product NDC: 54575-339
Proprietary Name: BANANA
Non Proprietary Name: banana
Active Ingredient(s): 1    g/20mL & nbsp;   banana
Administration Route(s): PERCUTANEOUS; SUBCUTANEOUS
Dosage Form(s): INJECTION, SOLUTION
Coding System: National Drug Codes(NDC)

Labeler Information of BANANA

Product NDC: 54575-339
Labeler Name: Allergy Laboratories, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: BLA101376
Marketing Category: BLA
Start Marketing Date: 19671207

Package Information of BANANA

Package NDC: 54575-339-02
Package Description: 2 mL in 1 VIAL, MULTI-DOSE (54575-339-02)

NDC Information of BANANA

NDC Code 54575-339-02
Proprietary Name BANANA
Package Description 2 mL in 1 VIAL, MULTI-DOSE (54575-339-02)
Product NDC 54575-339
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name banana
Dosage Form Name INJECTION, SOLUTION
Route Name PERCUTANEOUS; SUBCUTANEOUS
Start Marketing Date 19671207
Marketing Category Name BLA
Labeler Name Allergy Laboratories, Inc.
Substance Name BANANA
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],Fruit Proteins [Chemical/Ingredient]

Complete Information of BANANA


General Information