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Pussy Willow Pollen - 49643-407-10 - (Salix discolor)

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Drug Information of Pussy Willow Pollen

Product NDC: 49643-407
Proprietary Name: Pussy Willow Pollen
Non Proprietary Name: Salix discolor
Active Ingredient(s): 1    g/20mL & nbsp;   Salix discolor
Administration Route(s): CUTANEOUS; INTRADERMAL; SUBCUTANEOUS
Dosage Form(s): INJECTION
Coding System: National Drug Codes(NDC)

Labeler Information of Pussy Willow Pollen

Product NDC: 49643-407
Labeler Name: Allermed Laboratories, Inc.
Product Type: NON-STANDARDIZED ALLERGENIC
FDA Application Number: BLA102212
Marketing Category: BLA
Start Marketing Date: 19740312

Package Information of Pussy Willow Pollen

Package NDC: 49643-407-10
Package Description: 10 mL in 1 VIAL, MULTI-DOSE (49643-407-10)

NDC Information of Pussy Willow Pollen

NDC Code 49643-407-10
Proprietary Name Pussy Willow Pollen
Package Description 10 mL in 1 VIAL, MULTI-DOSE (49643-407-10)
Product NDC 49643-407
Product Type Name NON-STANDARDIZED ALLERGENIC
Non Proprietary Name Salix discolor
Dosage Form Name INJECTION
Route Name CUTANEOUS; INTRADERMAL; SUBCUTANEOUS
Start Marketing Date 19740312
Marketing Category Name BLA
Labeler Name Allermed Laboratories, Inc.
Substance Name SALIX DISCOLOR 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 Pussy Willow Pollen


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