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POA ANNUA POLLEN - 0268-6689-06 - (Annual Bluegrass)

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Drug Information of POA ANNUA POLLEN

Product NDC: 0268-6689
Proprietary Name: POA ANNUA POLLEN
Non Proprietary Name: Annual Bluegrass
Active Ingredient(s): .05    g/mL & nbsp;   Annual Bluegrass
Administration Route(s): PERCUTANEOUS
Dosage Form(s): INJECTION, SOLUTION
Coding System: National Drug Codes(NDC)

Labeler Information of POA ANNUA POLLEN

Product NDC: 0268-6689
Labeler Name: ALK-Abello, Inc.
Product Type: NON-STANDARDIZED ALLERGENIC
FDA Application Number: BLA103753
Marketing Category: BLA
Start Marketing Date: 19650101

Package Information of POA ANNUA POLLEN

Package NDC: 0268-6689-06
Package Description: 5 mL in 1 VIAL, MULTI-DOSE (0268-6689-06)

NDC Information of POA ANNUA POLLEN

NDC Code 0268-6689-06
Proprietary Name POA ANNUA POLLEN
Package Description 5 mL in 1 VIAL, MULTI-DOSE (0268-6689-06)
Product NDC 0268-6689
Product Type Name NON-STANDARDIZED ALLERGENIC
Non Proprietary Name Annual Bluegrass
Dosage Form Name INJECTION, SOLUTION
Route Name PERCUTANEOUS
Start Marketing Date 19650101
Marketing Category Name BLA
Labeler Name ALK-Abello, Inc.
Substance Name POA ANNUA POLLEN
Strength Number .05
Strength Unit g/mL
Pharmaceutical Classes 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 POA ANNUA POLLEN


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