Tuna - 49288-0569-3 - (Tuna)

Alphabetical Index


Drug Information of Tuna

Product NDC: 49288-0569
Proprietary Name: Tuna
Non Proprietary Name: Tuna
Active Ingredient(s): .05    g/mL & nbsp;   Tuna
Administration Route(s): INTRADERMAL; SUBCUTANEOUS
Dosage Form(s): INJECTION, SOLUTION
Coding System: National Drug Codes(NDC)

Labeler Information of Tuna

Product NDC: 49288-0569
Labeler Name: Antigen Laboratories, Inc.
Product Type: NON-STANDARDIZED ALLERGENIC
FDA Application Number: BLA102223
Marketing Category: BLA
Start Marketing Date: 19740323

Package Information of Tuna

Package NDC: 49288-0569-3
Package Description: 10 mL in 1 VIAL, MULTI-DOSE (49288-0569-3)

NDC Information of Tuna

NDC Code 49288-0569-3
Proprietary Name Tuna
Package Description 10 mL in 1 VIAL, MULTI-DOSE (49288-0569-3)
Product NDC 49288-0569
Product Type Name NON-STANDARDIZED ALLERGENIC
Non Proprietary Name Tuna
Dosage Form Name INJECTION, SOLUTION
Route Name INTRADERMAL; SUBCUTANEOUS
Start Marketing Date 19740323
Marketing Category Name BLA
Labeler Name Antigen Laboratories, Inc.
Substance Name TUNA
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 Tuna


General Information