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Standardized Kentucky (June) Bluegrass - 49288-0277-3 - (Standardized Kentucky (June) Bluegrass)

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Drug Information of Standardized Kentucky (June) Bluegrass

Product NDC: 49288-0277
Proprietary Name: Standardized Kentucky (June) Bluegrass
Non Proprietary Name: Standardized Kentucky (June) Bluegrass
Active Ingredient(s): 100000    [BAU]/mL & nbsp;   Standardized Kentucky (June) Bluegrass
Administration Route(s): INTRADERMAL; SUBCUTANEOUS
Dosage Form(s): INJECTION, SOLUTION
Coding System: National Drug Codes(NDC)

Labeler Information of Standardized Kentucky (June) Bluegrass

Product NDC: 49288-0277
Labeler Name: Antigen Laboratories, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: BLA103421
Marketing Category: BLA
Start Marketing Date: 19970613

Package Information of Standardized Kentucky (June) Bluegrass

Package NDC: 49288-0277-3
Package Description: 10 mL in 1 VIAL, MULTI-DOSE (49288-0277-3)

NDC Information of Standardized Kentucky (June) Bluegrass

NDC Code 49288-0277-3
Proprietary Name Standardized Kentucky (June) Bluegrass
Package Description 10 mL in 1 VIAL, MULTI-DOSE (49288-0277-3)
Product NDC 49288-0277
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Standardized Kentucky (June) Bluegrass
Dosage Form Name INJECTION, SOLUTION
Route Name INTRADERMAL; SUBCUTANEOUS
Start Marketing Date 19970613
Marketing Category Name BLA
Labeler Name Antigen Laboratories, Inc.
Substance Name POA PRATENSIS 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 Standardized Kentucky (June) Bluegrass


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