Home > National Drug Code (NDC) > QUERCUS ALBA POLLEN

QUERCUS ALBA POLLEN - 0268-1331-10 - (Oak White)

Alphabetical Index


Drug Information of QUERCUS ALBA POLLEN

Product NDC: 0268-1331
Proprietary Name: QUERCUS ALBA POLLEN
Non Proprietary Name: Oak White
Active Ingredient(s): 20000    [PNU]/mL & nbsp;   Oak White
Administration Route(s): SUBCUTANEOUS
Dosage Form(s): INJECTION, SOLUTION
Coding System: National Drug Codes(NDC)

Labeler Information of QUERCUS ALBA POLLEN

Product NDC: 0268-1331
Labeler Name: ALK-Abello, Inc.
Product Type: NON-STANDARDIZED ALLERGENIC
FDA Application Number: BLA103753
Marketing Category: BLA
Start Marketing Date: 19650101

Package Information of QUERCUS ALBA POLLEN

Package NDC: 0268-1331-10
Package Description: 10 mL in 1 VIAL, MULTI-DOSE (0268-1331-10)

NDC Information of QUERCUS ALBA POLLEN

NDC Code 0268-1331-10
Proprietary Name QUERCUS ALBA POLLEN
Package Description 10 mL in 1 VIAL, MULTI-DOSE (0268-1331-10)
Product NDC 0268-1331
Product Type Name NON-STANDARDIZED ALLERGENIC
Non Proprietary Name Oak White
Dosage Form Name INJECTION, SOLUTION
Route Name SUBCUTANEOUS
Start Marketing Date 19650101
Marketing Category Name BLA
Labeler Name ALK-Abello, Inc.
Substance Name QUERCUS ALBA POLLEN
Strength Number 20000
Strength Unit [PNU]/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 QUERCUS ALBA POLLEN


General Information