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Timothy, Standardized - 0268-0279-10 - (Timothy, Standardized)

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Drug Information of Timothy, Standardized

Product NDC: 0268-0279
Proprietary Name: Timothy, Standardized
Non Proprietary Name: Timothy, Standardized
Active Ingredient(s): 100000    [BAU]/mL & nbsp;   Timothy, Standardized
Administration Route(s): SUBCUTANEOUS
Dosage Form(s): INJECTION, SOLUTION
Coding System: National Drug Codes(NDC)

Labeler Information of Timothy, Standardized

Product NDC: 0268-0279
Labeler Name: ALK-Abello, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: BLA103058
Marketing Category: BLA
Start Marketing Date: 19971218

Package Information of Timothy, Standardized

Package NDC: 0268-0279-10
Package Description: 10 mL in 1 VIAL, MULTI-DOSE (0268-0279-10)

NDC Information of Timothy, Standardized

NDC Code 0268-0279-10
Proprietary Name Timothy, Standardized
Package Description 10 mL in 1 VIAL, MULTI-DOSE (0268-0279-10)
Product NDC 0268-0279
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Timothy, Standardized
Dosage Form Name INJECTION, SOLUTION
Route Name SUBCUTANEOUS
Start Marketing Date 19971218
Marketing Category Name BLA
Labeler Name ALK-Abello, Inc.
Substance Name PHLEUM PRATENSE POLLEN
Strength Number 100000
Strength Unit [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]

Complete Information of Timothy, Standardized


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