RABBIT - 0268-0650-50 - (RABBIT)

Alphabetical Index


Drug Information of RABBIT

Product NDC: 0268-0650
Proprietary Name: RABBIT
Non Proprietary Name: RABBIT
Active Ingredient(s): .1    g/mL & nbsp;   RABBIT
Administration Route(s): SUBCUTANEOUS
Dosage Form(s): INJECTION, SOLUTION
Coding System: National Drug Codes(NDC)

Labeler Information of RABBIT

Product NDC: 0268-0650
Labeler Name: ALK-Abello, Inc.
Product Type: NON-STANDARDIZED ALLERGENIC
FDA Application Number: BLA103753
Marketing Category: BLA
Start Marketing Date: 19650101

Package Information of RABBIT

Package NDC: 0268-0650-50
Package Description: 50 mL in 1 VIAL, MULTI-DOSE (0268-0650-50)

NDC Information of RABBIT

NDC Code 0268-0650-50
Proprietary Name RABBIT
Package Description 50 mL in 1 VIAL, MULTI-DOSE (0268-0650-50)
Product NDC 0268-0650
Product Type Name NON-STANDARDIZED ALLERGENIC
Non Proprietary Name RABBIT
Dosage Form Name INJECTION, SOLUTION
Route Name SUBCUTANEOUS
Start Marketing Date 19650101
Marketing Category Name BLA
Labeler Name ALK-Abello, Inc.
Substance Name RABBIT
Strength Number .1
Strength Unit g/mL
Pharmaceutical Classes Non-Standardized Food Allergenic Extract [EPC],Increased Histamine Release [PE],Cell-mediated Immunity [PE],Allergens [Chemical/Ingredient],Dietary Proteins [Chemical/Ingredient],Meat Proteins [Chemical/Ingredient]

Complete Information of RABBIT


General Information