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Kentucky Bluegrass (June), Standardized - 0268-0284-10 - (Kentucky Bluegrass (June), Standardized)

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Drug Information of Kentucky Bluegrass (June), Standardized

Product NDC: 0268-0284
Proprietary Name: Kentucky Bluegrass (June), Standardized
Non Proprietary Name: Kentucky Bluegrass (June), Standardized
Active Ingredient(s): 10000    [BAU]/mL & nbsp;   Kentucky Bluegrass (June), Standardized
Administration Route(s): SUBCUTANEOUS
Dosage Form(s): INJECTION, SOLUTION
Coding System: National Drug Codes(NDC)

Labeler Information of Kentucky Bluegrass (June), Standardized

Product NDC: 0268-0284
Labeler Name: ALK-Abello, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: BLA103052
Marketing Category: BLA
Start Marketing Date: 19971218

Package Information of Kentucky Bluegrass (June), Standardized

Package NDC: 0268-0284-10
Package Description: 10 mL in 1 VIAL, MULTI-DOSE (0268-0284-10)

NDC Information of Kentucky Bluegrass (June), Standardized

NDC Code 0268-0284-10
Proprietary Name Kentucky Bluegrass (June), Standardized
Package Description 10 mL in 1 VIAL, MULTI-DOSE (0268-0284-10)
Product NDC 0268-0284
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Kentucky Bluegrass (June), Standardized
Dosage Form Name INJECTION, SOLUTION
Route Name SUBCUTANEOUS
Start Marketing Date 19971218
Marketing Category Name BLA
Labeler Name ALK-Abello, Inc.
Substance Name POA PRATENSIS POLLEN
Strength Number 10000
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 Kentucky Bluegrass (June), Standardized


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