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White Poplar Pollen - 49643-394-30 - (Populus alba)

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Drug Information of White Poplar Pollen

Product NDC: 49643-394
Proprietary Name: White Poplar Pollen
Non Proprietary Name: Populus alba
Active Ingredient(s): 1    g/20mL & nbsp;   Populus alba
Administration Route(s): CUTANEOUS; INTRADERMAL; SUBCUTANEOUS
Dosage Form(s): INJECTION
Coding System: National Drug Codes(NDC)

Labeler Information of White Poplar Pollen

Product NDC: 49643-394
Labeler Name: Allermed Laboratories, Inc.
Product Type: NON-STANDARDIZED ALLERGENIC
FDA Application Number: BLA102212
Marketing Category: BLA
Start Marketing Date: 19740312

Package Information of White Poplar Pollen

Package NDC: 49643-394-30
Package Description: 30 mL in 1 VIAL, MULTI-DOSE (49643-394-30)

NDC Information of White Poplar Pollen

NDC Code 49643-394-30
Proprietary Name White Poplar Pollen
Package Description 30 mL in 1 VIAL, MULTI-DOSE (49643-394-30)
Product NDC 49643-394
Product Type Name NON-STANDARDIZED ALLERGENIC
Non Proprietary Name Populus alba
Dosage Form Name INJECTION
Route Name CUTANEOUS; INTRADERMAL; SUBCUTANEOUS
Start Marketing Date 19740312
Marketing Category Name BLA
Labeler Name Allermed Laboratories, Inc.
Substance Name POPULUS ALBA 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 White Poplar Pollen


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