Home > National Drug Code (NDC) > OLEA EUROPAEA POLLEN

OLEA EUROPAEA POLLEN - 0268-1340-50 - (Olive Pollen)

Alphabetical Index


Drug Information of OLEA EUROPAEA POLLEN

Product NDC: 0268-1340
Proprietary Name: OLEA EUROPAEA POLLEN
Non Proprietary Name: Olive Pollen
Active Ingredient(s): .05    g/mL & nbsp;   Olive Pollen
Administration Route(s): SUBCUTANEOUS
Dosage Form(s): INJECTION, SOLUTION
Coding System: National Drug Codes(NDC)

Labeler Information of OLEA EUROPAEA POLLEN

Product NDC: 0268-1340
Labeler Name: ALK-Abello, Inc.
Product Type: NON-STANDARDIZED ALLERGENIC
FDA Application Number: BLA103753
Marketing Category: BLA
Start Marketing Date: 19650101

Package Information of OLEA EUROPAEA POLLEN

Package NDC: 0268-1340-50
Package Description: 50 mL in 1 VIAL, MULTI-DOSE (0268-1340-50)

NDC Information of OLEA EUROPAEA POLLEN

NDC Code 0268-1340-50
Proprietary Name OLEA EUROPAEA POLLEN
Package Description 50 mL in 1 VIAL, MULTI-DOSE (0268-1340-50)
Product NDC 0268-1340
Product Type Name NON-STANDARDIZED ALLERGENIC
Non Proprietary Name Olive Pollen
Dosage Form Name INJECTION, SOLUTION
Route Name SUBCUTANEOUS
Start Marketing Date 19650101
Marketing Category Name BLA
Labeler Name ALK-Abello, Inc.
Substance Name OLEA EUROPAEA 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 OLEA EUROPAEA POLLEN


General Information