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Rabbitbush Pollen - 49643-354-10 - (Ambrosia deltoides)

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Drug Information of Rabbitbush Pollen

Product NDC: 49643-354
Proprietary Name: Rabbitbush Pollen
Non Proprietary Name: Ambrosia deltoides
Active Ingredient(s): 1    g/20mL & nbsp;   Ambrosia deltoides
Administration Route(s): CUTANEOUS; INTRADERMAL; SUBCUTANEOUS
Dosage Form(s): INJECTION
Coding System: National Drug Codes(NDC)

Labeler Information of Rabbitbush Pollen

Product NDC: 49643-354
Labeler Name: Allermed Laboratories, Inc.
Product Type: NON-STANDARDIZED ALLERGENIC
FDA Application Number: BLA102212
Marketing Category: BLA
Start Marketing Date: 19740312

Package Information of Rabbitbush Pollen

Package NDC: 49643-354-10
Package Description: 10 mL in 1 VIAL, MULTI-DOSE (49643-354-10)

NDC Information of Rabbitbush Pollen

NDC Code 49643-354-10
Proprietary Name Rabbitbush Pollen
Package Description 10 mL in 1 VIAL, MULTI-DOSE (49643-354-10)
Product NDC 49643-354
Product Type Name NON-STANDARDIZED ALLERGENIC
Non Proprietary Name Ambrosia deltoides
Dosage Form Name INJECTION
Route Name CUTANEOUS; INTRADERMAL; SUBCUTANEOUS
Start Marketing Date 19740312
Marketing Category Name BLA
Labeler Name Allermed Laboratories, Inc.
Substance Name AMBROSIA DELTOIDEA POLLEN
Strength Number 1
Strength Unit g/20mL
Pharmaceutical Classes Non-Standardized Pollen Allergenic Extract [EPC],Increased Histamine Release [PE],Cell-mediated Immunity [PE],Pollen [Chemical/Ingredient],Allergens [Chemical/Ingredient]

Complete Information of Rabbitbush Pollen


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