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Paecilomyces - 49288-0370-5 - (Paecilomyces)

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Drug Information of Paecilomyces

Product NDC: 49288-0370
Proprietary Name: Paecilomyces
Non Proprietary Name: Paecilomyces
Active Ingredient(s): .1    g/mL & nbsp;   Paecilomyces
Administration Route(s): INTRADERMAL; SUBCUTANEOUS
Dosage Form(s): INJECTION, SOLUTION
Coding System: National Drug Codes(NDC)

Labeler Information of Paecilomyces

Product NDC: 49288-0370
Labeler Name: Antigen Laboratories, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: BLA102223
Marketing Category: BLA
Start Marketing Date: 19920413

Package Information of Paecilomyces

Package NDC: 49288-0370-5
Package Description: 50 mL in 1 VIAL, MULTI-DOSE (49288-0370-5)

NDC Information of Paecilomyces

NDC Code 49288-0370-5
Proprietary Name Paecilomyces
Package Description 50 mL in 1 VIAL, MULTI-DOSE (49288-0370-5)
Product NDC 49288-0370
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Paecilomyces
Dosage Form Name INJECTION, SOLUTION
Route Name INTRADERMAL; SUBCUTANEOUS
Start Marketing Date 19920413
Marketing Category Name BLA
Labeler Name Antigen Laboratories, Inc.
Substance Name PAECILOMYCES VARIOTII
Strength Number .1
Strength Unit g/mL
Pharmaceutical Classes Non-Standardized Fungal Allergenic Extract [EPC],Increased Histamine Release [PE],Cell-mediated Immunity [PE],Increased IgG Production [PE],Fungal Proteins [Chemical/Ingredient],Allergens [Chemical/Ingredient]

Complete Information of Paecilomyces


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