Bluefish - 36987-1191-3 - (Bluefish)

Alphabetical Index


Drug Information of Bluefish

Product NDC: 36987-1191
Proprietary Name: Bluefish
Non Proprietary Name: Bluefish
Active Ingredient(s): .05    g/mL & nbsp;   Bluefish
Administration Route(s): INTRADERMAL; SUBCUTANEOUS
Dosage Form(s): INJECTION, SOLUTION
Coding System: National Drug Codes(NDC)

Labeler Information of Bluefish

Product NDC: 36987-1191
Labeler Name: Nelco Laboratories, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: BLA102192
Marketing Category: BLA
Start Marketing Date: 19720829

Package Information of Bluefish

Package NDC: 36987-1191-3
Package Description: 30 mL in 1 VIAL, MULTI-DOSE (36987-1191-3)

NDC Information of Bluefish

NDC Code 36987-1191-3
Proprietary Name Bluefish
Package Description 30 mL in 1 VIAL, MULTI-DOSE (36987-1191-3)
Product NDC 36987-1191
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Bluefish
Dosage Form Name INJECTION, SOLUTION
Route Name INTRADERMAL; SUBCUTANEOUS
Start Marketing Date 19720829
Marketing Category Name BLA
Labeler Name Nelco Laboratories, Inc.
Substance Name BLUEFISH
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 Bluefish


General Information