Home > National Drug Code (NDC) > Treatment Set TS335683

Treatment Set TS335683 - 49288-0781-3 - (Treatment Set TS335683)

Alphabetical Index


Drug Information of Treatment Set TS335683

Product NDC: 49288-0781
Proprietary Name: Treatment Set TS335683
Non Proprietary Name: Treatment Set TS335683
Active Ingredient(s): 2000; 20000    [BAU]/mL; [BAU]/mL & nbsp;   Treatment Set TS335683
Administration Route(s): INTRADERMAL; SUBCUTANEOUS
Dosage Form(s): INJECTION, SOLUTION
Coding System: National Drug Codes(NDC)

Labeler Information of Treatment Set TS335683

Product NDC: 49288-0781
Labeler Name: Antigen Laboratories, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: BLA102223
Marketing Category: BLA
Start Marketing Date: 19861031

Package Information of Treatment Set TS335683

Package NDC: 49288-0781-3
Package Description: 10 mL in 1 VIAL, MULTI-DOSE (49288-0781-3)

NDC Information of Treatment Set TS335683

NDC Code 49288-0781-3
Proprietary Name Treatment Set TS335683
Package Description 10 mL in 1 VIAL, MULTI-DOSE (49288-0781-3)
Product NDC 49288-0781
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Treatment Set TS335683
Dosage Form Name INJECTION, SOLUTION
Route Name INTRADERMAL; SUBCUTANEOUS
Start Marketing Date 19861031
Marketing Category Name BLA
Labeler Name Antigen Laboratories, Inc.
Substance Name CYNODON DACTYLON POLLEN; PHLEUM PRATENSE POLLEN
Strength Number 2000; 20000
Strength Unit [BAU]/mL; [BAU]/mL
Pharmaceutical Classes Standardized Pollen Allergenic Extract [EPC],Increased Histamine Release [PE],Cell-mediated Immunity [PE],Increased IgG Production [PE],Pollen [Chemical/Ingredient],Allergens [Chemical/Ingredient],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 TS335683


General Information