STRAWBERRY - 54575-462-10 - (strawberry)

Alphabetical Index


Drug Information of STRAWBERRY

Product NDC: 54575-462
Proprietary Name: STRAWBERRY
Non Proprietary Name: strawberry
Active Ingredient(s): 1    g/20mL & nbsp;   strawberry
Administration Route(s): PERCUTANEOUS; SUBCUTANEOUS
Dosage Form(s): INJECTION, SOLUTION
Coding System: National Drug Codes(NDC)

Labeler Information of STRAWBERRY

Product NDC: 54575-462
Labeler Name: Allergy Laboratories, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: BLA101376
Marketing Category: BLA
Start Marketing Date: 19671207

Package Information of STRAWBERRY

Package NDC: 54575-462-10
Package Description: 10 mL in 1 VIAL, MULTI-DOSE (54575-462-10)

NDC Information of STRAWBERRY

NDC Code 54575-462-10
Proprietary Name STRAWBERRY
Package Description 10 mL in 1 VIAL, MULTI-DOSE (54575-462-10)
Product NDC 54575-462
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name strawberry
Dosage Form Name INJECTION, SOLUTION
Route Name PERCUTANEOUS; SUBCUTANEOUS
Start Marketing Date 19671207
Marketing Category Name BLA
Labeler Name Allergy Laboratories, Inc.
Substance Name STRAWBERRY
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 STRAWBERRY


General Information