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HOLCUS LANATUS POLLEN - 0268-1511-10 - (Velvet Grass)

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Drug Information of HOLCUS LANATUS POLLEN

Product NDC: 0268-1511
Proprietary Name: HOLCUS LANATUS POLLEN
Non Proprietary Name: Velvet Grass
Active Ingredient(s): .05    g/mL & nbsp;   Velvet Grass
Administration Route(s): SUBCUTANEOUS
Dosage Form(s): INJECTION, SOLUTION
Coding System: National Drug Codes(NDC)

Labeler Information of HOLCUS LANATUS POLLEN

Product NDC: 0268-1511
Labeler Name: ALK-Abello, Inc.
Product Type: NON-STANDARDIZED ALLERGENIC
FDA Application Number: BLA103753
Marketing Category: BLA
Start Marketing Date: 19650101

Package Information of HOLCUS LANATUS POLLEN

Package NDC: 0268-1511-10
Package Description: 10 mL in 1 VIAL, MULTI-DOSE (0268-1511-10)

NDC Information of HOLCUS LANATUS POLLEN

NDC Code 0268-1511-10
Proprietary Name HOLCUS LANATUS POLLEN
Package Description 10 mL in 1 VIAL, MULTI-DOSE (0268-1511-10)
Product NDC 0268-1511
Product Type Name NON-STANDARDIZED ALLERGENIC
Non Proprietary Name Velvet Grass
Dosage Form Name INJECTION, SOLUTION
Route Name SUBCUTANEOUS
Start Marketing Date 19650101
Marketing Category Name BLA
Labeler Name ALK-Abello, Inc.
Substance Name HOLCUS LANATUS 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],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 HOLCUS LANATUS POLLEN


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