Haddock - 49288-0250-1 - (Haddock)

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Drug Information of Haddock

Product NDC: 49288-0250
Proprietary Name: Haddock
Non Proprietary Name: Haddock
Active Ingredient(s): .05    g/mL & nbsp;   Haddock
Administration Route(s): INTRADERMAL; SUBCUTANEOUS
Dosage Form(s): INJECTION, SOLUTION
Coding System: National Drug Codes(NDC)

Labeler Information of Haddock

Product NDC: 49288-0250
Labeler Name: Antigen Laboratories, Inc.
Product Type: NON-STANDARDIZED ALLERGENIC
FDA Application Number: BLA102223
Marketing Category: BLA
Start Marketing Date: 19740323

Package Information of Haddock

Package NDC: 49288-0250-1
Package Description: 2 mL in 1 VIAL, MULTI-DOSE (49288-0250-1)

NDC Information of Haddock

NDC Code 49288-0250-1
Proprietary Name Haddock
Package Description 2 mL in 1 VIAL, MULTI-DOSE (49288-0250-1)
Product NDC 49288-0250
Product Type Name NON-STANDARDIZED ALLERGENIC
Non Proprietary Name Haddock
Dosage Form Name INJECTION, SOLUTION
Route Name INTRADERMAL; SUBCUTANEOUS
Start Marketing Date 19740323
Marketing Category Name BLA
Labeler Name Antigen Laboratories, Inc.
Substance Name HADDOCK
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 Haddock


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