Tuna Fish - 36987-1274-2 - (Tuna Fish)

Alphabetical Index


Drug Information of Tuna Fish

Product NDC: 36987-1274
Proprietary Name: Tuna Fish
Non Proprietary Name: Tuna Fish
Active Ingredient(s): .05    g/mL & nbsp;   Tuna Fish
Administration Route(s): INTRADERMAL; SUBCUTANEOUS
Dosage Form(s): INJECTION, SOLUTION
Coding System: National Drug Codes(NDC)

Labeler Information of Tuna Fish

Product NDC: 36987-1274
Labeler Name: Nelco Laboratories, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: BLA102192
Marketing Category: BLA
Start Marketing Date: 19720829

Package Information of Tuna Fish

Package NDC: 36987-1274-2
Package Description: 10 mL in 1 VIAL, MULTI-DOSE (36987-1274-2)

NDC Information of Tuna Fish

NDC Code 36987-1274-2
Proprietary Name Tuna Fish
Package Description 10 mL in 1 VIAL, MULTI-DOSE (36987-1274-2)
Product NDC 36987-1274
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Tuna Fish
Dosage Form Name INJECTION, SOLUTION
Route Name INTRADERMAL; SUBCUTANEOUS
Start Marketing Date 19720829
Marketing Category Name BLA
Labeler Name Nelco 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 Fish


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