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Redtop Grass, Standardized - 0268-0286-10 - (Redtop Grass, Standardized)

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Drug Information of Redtop Grass, Standardized

Product NDC: 0268-0286
Proprietary Name: Redtop Grass, Standardized
Non Proprietary Name: Redtop Grass, Standardized
Active Ingredient(s): 10000    [BAU]/mL & nbsp;   Redtop Grass, Standardized
Administration Route(s): SUBCUTANEOUS
Dosage Form(s): INJECTION, SOLUTION
Coding System: National Drug Codes(NDC)

Labeler Information of Redtop Grass, Standardized

Product NDC: 0268-0286
Labeler Name: ALK-Abello, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: BLA103055
Marketing Category: BLA
Start Marketing Date: 19971218

Package Information of Redtop Grass, Standardized

Package NDC: 0268-0286-10
Package Description: 10 mL in 1 VIAL, MULTI-DOSE (0268-0286-10)

NDC Information of Redtop Grass, Standardized

NDC Code 0268-0286-10
Proprietary Name Redtop Grass, Standardized
Package Description 10 mL in 1 VIAL, MULTI-DOSE (0268-0286-10)
Product NDC 0268-0286
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Redtop Grass, Standardized
Dosage Form Name INJECTION, SOLUTION
Route Name SUBCUTANEOUS
Start Marketing Date 19971218
Marketing Category Name BLA
Labeler Name ALK-Abello, Inc.
Substance Name AGROSTIS GIGANTEA POLLEN
Strength Number 10000
Strength Unit [BAU]/mL
Pharmaceutical Classes Standardized Pollen Allergenic Extract [EPC],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 Redtop Grass, Standardized


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