Orange - 49288-0333-2 - (Orange)

Alphabetical Index


Drug Information of Orange

Product NDC: 49288-0333
Proprietary Name: Orange
Non Proprietary Name: Orange
Active Ingredient(s): 1    mL/mL & nbsp;   Orange
Administration Route(s): INTRADERMAL; SUBCUTANEOUS
Dosage Form(s): INJECTION, SOLUTION
Coding System: National Drug Codes(NDC)

Labeler Information of Orange

Product NDC: 49288-0333
Labeler Name: Antigen Laboratories, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: BLA102223
Marketing Category: BLA
Start Marketing Date: 19740323

Package Information of Orange

Package NDC: 49288-0333-2
Package Description: 5 mL in 1 VIAL, MULTI-DOSE (49288-0333-2)

NDC Information of Orange

NDC Code 49288-0333-2
Proprietary Name Orange
Package Description 5 mL in 1 VIAL, MULTI-DOSE (49288-0333-2)
Product NDC 49288-0333
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Orange
Dosage Form Name INJECTION, SOLUTION
Route Name INTRADERMAL; SUBCUTANEOUS
Start Marketing Date 19740323
Marketing Category Name BLA
Labeler Name Antigen Laboratories, Inc.
Substance Name ORANGE
Strength Number 1
Strength Unit mL/mL
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 Orange


General Information