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PAPER MULBERRY POLLEN - 54575-945-50 - (broussonetia papyrifera pollen)

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Drug Information of PAPER MULBERRY POLLEN

Product NDC: 54575-945
Proprietary Name: PAPER MULBERRY POLLEN
Non Proprietary Name: broussonetia papyrifera pollen
Active Ingredient(s): 1    g/20mL & nbsp;   broussonetia papyrifera pollen
Administration Route(s): PERCUTANEOUS; SUBCUTANEOUS
Dosage Form(s): INJECTION, SOLUTION
Coding System: National Drug Codes(NDC)

Labeler Information of PAPER MULBERRY POLLEN

Product NDC: 54575-945
Labeler Name: Allergy Laboratories, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: BLA101376
Marketing Category: BLA
Start Marketing Date: 19671207

Package Information of PAPER MULBERRY POLLEN

Package NDC: 54575-945-50
Package Description: 50 mL in 1 VIAL, MULTI-DOSE (54575-945-50)

NDC Information of PAPER MULBERRY POLLEN

NDC Code 54575-945-50
Proprietary Name PAPER MULBERRY POLLEN
Package Description 50 mL in 1 VIAL, MULTI-DOSE (54575-945-50)
Product NDC 54575-945
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name broussonetia papyrifera pollen
Dosage Form Name INJECTION, SOLUTION
Route Name PERCUTANEOUS; SUBCUTANEOUS
Start Marketing Date 19671207
Marketing Category Name BLA
Labeler Name Allergy Laboratories, Inc.
Substance Name BROUSSONETIA PAPYRIFERA 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 PAPER MULBERRY POLLEN


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