Halibut - 36987-1219-4 - (Halibut)

Alphabetical Index


Drug Information of Halibut

Product NDC: 36987-1219
Proprietary Name: Halibut
Non Proprietary Name: Halibut
Active Ingredient(s): .05    g/mL & nbsp;   Halibut
Administration Route(s): INTRADERMAL; SUBCUTANEOUS
Dosage Form(s): INJECTION, SOLUTION
Coding System: National Drug Codes(NDC)

Labeler Information of Halibut

Product NDC: 36987-1219
Labeler Name: Nelco Laboratories, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: BLA102192
Marketing Category: BLA
Start Marketing Date: 19720829

Package Information of Halibut

Package NDC: 36987-1219-4
Package Description: 50 mL in 1 VIAL, MULTI-DOSE (36987-1219-4)

NDC Information of Halibut

NDC Code 36987-1219-4
Proprietary Name Halibut
Package Description 50 mL in 1 VIAL, MULTI-DOSE (36987-1219-4)
Product NDC 36987-1219
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Halibut
Dosage Form Name INJECTION, SOLUTION
Route Name INTRADERMAL; SUBCUTANEOUS
Start Marketing Date 19720829
Marketing Category Name BLA
Labeler Name Nelco Laboratories, Inc.
Substance Name PACIFIC HALIBUT
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 Halibut


General Information