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Standardized Kentucky Blue (June) Grass - 49643-393-50 - (Poa pratensis)

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Drug Information of Standardized Kentucky Blue (June) Grass

Product NDC: 49643-393
Proprietary Name: Standardized Kentucky Blue (June) Grass
Non Proprietary Name: Poa pratensis
Active Ingredient(s): 100000    [BAU]/mL & nbsp;   Poa pratensis
Administration Route(s): CUTANEOUS; INTRADERMAL; SUBCUTANEOUS
Dosage Form(s): INJECTION
Coding System: National Drug Codes(NDC)

Labeler Information of Standardized Kentucky Blue (June) Grass

Product NDC: 49643-393
Labeler Name: Allermed Laboratories, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: BLA102215
Marketing Category: BLA
Start Marketing Date: 19961202

Package Information of Standardized Kentucky Blue (June) Grass

Package NDC: 49643-393-50
Package Description: 50 mL in 1 VIAL, MULTI-DOSE (49643-393-50)

NDC Information of Standardized Kentucky Blue (June) Grass

NDC Code 49643-393-50
Proprietary Name Standardized Kentucky Blue (June) Grass
Package Description 50 mL in 1 VIAL, MULTI-DOSE (49643-393-50)
Product NDC 49643-393
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Poa pratensis
Dosage Form Name INJECTION
Route Name CUTANEOUS; INTRADERMAL; SUBCUTANEOUS
Start Marketing Date 19961202
Marketing Category Name BLA
Labeler Name Allermed Laboratories, Inc.
Substance Name POA PRATENSIS POLLEN
Strength Number 100000
Strength Unit [BAU]/mL
Pharmaceutical Classes 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 Standardized Kentucky Blue (June) Grass


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