VANILLA - 54575-471-02 - (vanilla)

Alphabetical Index


Drug Information of VANILLA

Product NDC: 54575-471
Proprietary Name: VANILLA
Non Proprietary Name: vanilla
Active Ingredient(s): 1    g/20mL & nbsp;   vanilla
Administration Route(s): PERCUTANEOUS; SUBCUTANEOUS
Dosage Form(s): INJECTION, SOLUTION
Coding System: National Drug Codes(NDC)

Labeler Information of VANILLA

Product NDC: 54575-471
Labeler Name: Allergy Laboratories, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: BLA102192
Marketing Category: BLA
Start Marketing Date: 19720829

Package Information of VANILLA

Package NDC: 54575-471-02
Package Description: 2 mL in 1 VIAL, MULTI-DOSE (54575-471-02)

NDC Information of VANILLA

NDC Code 54575-471-02
Proprietary Name VANILLA
Package Description 2 mL in 1 VIAL, MULTI-DOSE (54575-471-02)
Product NDC 54575-471
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name vanilla
Dosage Form Name INJECTION, SOLUTION
Route Name PERCUTANEOUS; SUBCUTANEOUS
Start Marketing Date 19720829
Marketing Category Name BLA
Labeler Name Allergy Laboratories, Inc.
Substance Name VANILLA
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],Dietary Proteins [Chemical/Ingredient],Allergens [Chemical/Ingredient]

Complete Information of VANILLA


General Information