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MORUS RUBRA POLLEN - 0268-1306-10 - (Mulberry Red)

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Drug Information of MORUS RUBRA POLLEN

Product NDC: 0268-1306
Proprietary Name: MORUS RUBRA POLLEN
Non Proprietary Name: Mulberry Red
Active Ingredient(s): 40000    [PNU]/mL & nbsp;   Mulberry Red
Administration Route(s): SUBCUTANEOUS
Dosage Form(s): INJECTION, SOLUTION
Coding System: National Drug Codes(NDC)

Labeler Information of MORUS RUBRA POLLEN

Product NDC: 0268-1306
Labeler Name: ALK-Abello, Inc.
Product Type: NON-STANDARDIZED ALLERGENIC
FDA Application Number: BLA103753
Marketing Category: BLA
Start Marketing Date: 19650101

Package Information of MORUS RUBRA POLLEN

Package NDC: 0268-1306-10
Package Description: 10 mL in 1 VIAL, MULTI-DOSE (0268-1306-10)

NDC Information of MORUS RUBRA POLLEN

NDC Code 0268-1306-10
Proprietary Name MORUS RUBRA POLLEN
Package Description 10 mL in 1 VIAL, MULTI-DOSE (0268-1306-10)
Product NDC 0268-1306
Product Type Name NON-STANDARDIZED ALLERGENIC
Non Proprietary Name Mulberry Red
Dosage Form Name INJECTION, SOLUTION
Route Name SUBCUTANEOUS
Start Marketing Date 19650101
Marketing Category Name BLA
Labeler Name ALK-Abello, Inc.
Substance Name MORUS RUBRA POLLEN
Strength Number 40000
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 MORUS RUBRA POLLEN


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