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Treatment Set TS342034 - 49288-0819-3 - (Treatment Set TS342034)

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Drug Information of Treatment Set TS342034

Product NDC: 49288-0819
Proprietary Name: Treatment Set TS342034
Non Proprietary Name: Treatment Set TS342034
Active Ingredient(s): .01; .01    g/mL; g/mL & nbsp;   Treatment Set TS342034
Administration Route(s): INTRADERMAL; SUBCUTANEOUS
Dosage Form(s): INJECTION, SOLUTION
Coding System: National Drug Codes(NDC)

Labeler Information of Treatment Set TS342034

Product NDC: 49288-0819
Labeler Name: Antigen Laboratories, Inc.
Product Type: NON-STANDARDIZED ALLERGENIC
FDA Application Number: BLA102223
Marketing Category: BLA
Start Marketing Date: 19861031

Package Information of Treatment Set TS342034

Package NDC: 49288-0819-3
Package Description: 10 mL in 1 VIAL, MULTI-DOSE (49288-0819-3)

NDC Information of Treatment Set TS342034

NDC Code 49288-0819-3
Proprietary Name Treatment Set TS342034
Package Description 10 mL in 1 VIAL, MULTI-DOSE (49288-0819-3)
Product NDC 49288-0819
Product Type Name NON-STANDARDIZED ALLERGENIC
Non Proprietary Name Treatment Set TS342034
Dosage Form Name INJECTION, SOLUTION
Route Name INTRADERMAL; SUBCUTANEOUS
Start Marketing Date 19861031
Marketing Category Name BLA
Labeler Name Antigen Laboratories, Inc.
Substance Name CANIS LUPUS FAMILIARIS HAIR; PLANTAGO LANCEOLATA POLLEN
Strength Number .01; .01
Strength Unit g/mL; g/mL
Pharmaceutical Classes Non-Standardized Animal Hair Allergenic Extract [EPC],Increased Histamine Release [PE],Cell-mediated Immunity [PE],Increased IgG Production [PE],Fur [Chemical/Ingredient],Allergens [Chemical/Ingredient],Non-Standardized Pollen Allergenic Extract [EPC],Increased Histamine Release [PE],Cell-mediated Immunity [PE],Increased IgG Production [PE],Pollen [Chemical/Ingredient],Allergens [Chemical/Ingredient]

Complete Information of Treatment Set TS342034


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