FLOUNDER - 0268-6137-06 - (Flounder)

Alphabetical Index


Drug Information of FLOUNDER

Product NDC: 0268-6137
Proprietary Name: FLOUNDER
Non Proprietary Name: Flounder
Active Ingredient(s): .1    g/mL & nbsp;   Flounder
Administration Route(s): PERCUTANEOUS
Dosage Form(s): INJECTION, SOLUTION
Coding System: National Drug Codes(NDC)

Labeler Information of FLOUNDER

Product NDC: 0268-6137
Labeler Name: ALK-Abello, Inc.
Product Type: NON-STANDARDIZED ALLERGENIC
FDA Application Number: BLA103753
Marketing Category: BLA
Start Marketing Date: 19650101

Package Information of FLOUNDER

Package NDC: 0268-6137-06
Package Description: 5 mL in 1 VIAL, MULTI-DOSE (0268-6137-06)

NDC Information of FLOUNDER

NDC Code 0268-6137-06
Proprietary Name FLOUNDER
Package Description 5 mL in 1 VIAL, MULTI-DOSE (0268-6137-06)
Product NDC 0268-6137
Product Type Name NON-STANDARDIZED ALLERGENIC
Non Proprietary Name Flounder
Dosage Form Name INJECTION, SOLUTION
Route Name PERCUTANEOUS
Start Marketing Date 19650101
Marketing Category Name BLA
Labeler Name ALK-Abello, Inc.
Substance Name FLOUNDER
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],Fish Proteins, Dietary [Chemical/Ingredient]

Complete Information of FLOUNDER


General Information