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Hackberry Pollen - 49643-336-05 - (Celtis occidentalis)

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Drug Information of Hackberry Pollen

Product NDC: 49643-336
Proprietary Name: Hackberry Pollen
Non Proprietary Name: Celtis occidentalis
Active Ingredient(s): 1    g/20mL & nbsp;   Celtis occidentalis
Administration Route(s): CUTANEOUS; INTRADERMAL; SUBCUTANEOUS
Dosage Form(s): INJECTION
Coding System: National Drug Codes(NDC)

Labeler Information of Hackberry Pollen

Product NDC: 49643-336
Labeler Name: Allermed Laboratories, Inc.
Product Type: NON-STANDARDIZED ALLERGENIC
FDA Application Number: BLA102212
Marketing Category: BLA
Start Marketing Date: 19740312

Package Information of Hackberry Pollen

Package NDC: 49643-336-05
Package Description: 5 mL in 1 VIAL, MULTI-DOSE (49643-336-05)

NDC Information of Hackberry Pollen

NDC Code 49643-336-05
Proprietary Name Hackberry Pollen
Package Description 5 mL in 1 VIAL, MULTI-DOSE (49643-336-05)
Product NDC 49643-336
Product Type Name NON-STANDARDIZED ALLERGENIC
Non Proprietary Name Celtis occidentalis
Dosage Form Name INJECTION
Route Name CUTANEOUS; INTRADERMAL; SUBCUTANEOUS
Start Marketing Date 19740312
Marketing Category Name BLA
Labeler Name Allermed Laboratories, Inc.
Substance Name CELTIS OCCIDENTALIS POLLEN
Strength Number 1
Strength Unit g/20mL
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 Hackberry Pollen


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