RABBIT - 0268-0652-10 - (RABBIT)

Alphabetical Index


Drug Information of RABBIT

Product NDC: 0268-0652
Proprietary Name: RABBIT
Non Proprietary Name: RABBIT
Active Ingredient(s): 20000    [PNU]/mL & nbsp;   RABBIT
Administration Route(s): SUBCUTANEOUS
Dosage Form(s): INJECTION, SOLUTION
Coding System: National Drug Codes(NDC)

Labeler Information of RABBIT

Product NDC: 0268-0652
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: 0268-0652-10
Package Description: 10 mL in 1 VIAL, MULTI-DOSE (0268-0652-10)

NDC Information of RABBIT

NDC Code 0268-0652-10
Proprietary Name RABBIT
Package Description 10 mL in 1 VIAL, MULTI-DOSE (0268-0652-10)
Product NDC 0268-0652
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 20000
Strength Unit [PNU]/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