Salmon - 49288-0476-1 - (Salmon)

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Drug Information of Salmon

Product NDC: 49288-0476
Proprietary Name: Salmon
Non Proprietary Name: Salmon
Active Ingredient(s): .05    g/mL & nbsp;   Salmon
Administration Route(s): INTRADERMAL; SUBCUTANEOUS
Dosage Form(s): INJECTION, SOLUTION
Coding System: National Drug Codes(NDC)

Labeler Information of Salmon

Product NDC: 49288-0476
Labeler Name: Antigen Laboratories, Inc.
Product Type: NON-STANDARDIZED ALLERGENIC
FDA Application Number: BLA102223
Marketing Category: BLA
Start Marketing Date: 19740323

Package Information of Salmon

Package NDC: 49288-0476-1
Package Description: 2 mL in 1 VIAL, MULTI-DOSE (49288-0476-1)

NDC Information of Salmon

NDC Code 49288-0476-1
Proprietary Name Salmon
Package Description 2 mL in 1 VIAL, MULTI-DOSE (49288-0476-1)
Product NDC 49288-0476
Product Type Name NON-STANDARDIZED ALLERGENIC
Non Proprietary Name Salmon
Dosage Form Name INJECTION, SOLUTION
Route Name INTRADERMAL; SUBCUTANEOUS
Start Marketing Date 19740323
Marketing Category Name BLA
Labeler Name Antigen Laboratories, Inc.
Substance Name ATLANTIC SALMON
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 Salmon


General Information