White Fish - 49288-0599-4 - (White Fish)

Alphabetical Index


Drug Information of White Fish

Product NDC: 49288-0599
Proprietary Name: White Fish
Non Proprietary Name: White Fish
Active Ingredient(s): .05    g/mL & nbsp;   White Fish
Administration Route(s): INTRADERMAL; SUBCUTANEOUS
Dosage Form(s): INJECTION, SOLUTION
Coding System: National Drug Codes(NDC)

Labeler Information of White Fish

Product NDC: 49288-0599
Labeler Name: Antigen Laboratories, Inc.
Product Type: NON-STANDARDIZED ALLERGENIC
FDA Application Number: BLA102223
Marketing Category: BLA
Start Marketing Date: 19740323

Package Information of White Fish

Package NDC: 49288-0599-4
Package Description: 30 mL in 1 VIAL, MULTI-DOSE (49288-0599-4)

NDC Information of White Fish

NDC Code 49288-0599-4
Proprietary Name White Fish
Package Description 30 mL in 1 VIAL, MULTI-DOSE (49288-0599-4)
Product NDC 49288-0599
Product Type Name NON-STANDARDIZED ALLERGENIC
Non Proprietary Name White Fish
Dosage Form Name INJECTION, SOLUTION
Route Name INTRADERMAL; SUBCUTANEOUS
Start Marketing Date 19740323
Marketing Category Name BLA
Labeler Name Antigen Laboratories, Inc.
Substance Name WHITEFISH
Strength Number .05
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 White Fish


General Information