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White Poplar - 49288-0418-2 - (White Poplar)

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Drug Information of White Poplar

Product NDC: 49288-0418
Proprietary Name: White Poplar
Non Proprietary Name: White Poplar
Active Ingredient(s): .05    g/mL & nbsp;   White Poplar
Administration Route(s): INTRADERMAL; SUBCUTANEOUS
Dosage Form(s): INJECTION, SOLUTION
Coding System: National Drug Codes(NDC)

Labeler Information of White Poplar

Product NDC: 49288-0418
Labeler Name: Antigen Laboratories, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: BLA102223
Marketing Category: BLA
Start Marketing Date: 19740323

Package Information of White Poplar

Package NDC: 49288-0418-2
Package Description: 5 mL in 1 VIAL, MULTI-DOSE (49288-0418-2)

NDC Information of White Poplar

NDC Code 49288-0418-2
Proprietary Name White Poplar
Package Description 5 mL in 1 VIAL, MULTI-DOSE (49288-0418-2)
Product NDC 49288-0418
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name White Poplar
Dosage Form Name INJECTION, SOLUTION
Route Name INTRADERMAL; SUBCUTANEOUS
Start Marketing Date 19740323
Marketing Category Name BLA
Labeler Name Antigen Laboratories, Inc.
Substance Name POPULUS ALBA POLLEN
Strength Number .05
Strength Unit g/mL
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


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