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Mucor plumbeus - 36987-2006-3 - (Mucor plumbeus)

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Drug Information of Mucor plumbeus

Product NDC: 36987-2006
Proprietary Name: Mucor plumbeus
Non Proprietary Name: Mucor plumbeus
Active Ingredient(s): .05    g/mL & nbsp;   Mucor plumbeus
Administration Route(s): INTRADERMAL; SUBCUTANEOUS
Dosage Form(s): INJECTION, SOLUTION
Coding System: National Drug Codes(NDC)

Labeler Information of Mucor plumbeus

Product NDC: 36987-2006
Labeler Name: Nelco Laboratories, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: BLA102192
Marketing Category: BLA
Start Marketing Date: 19720829

Package Information of Mucor plumbeus

Package NDC: 36987-2006-3
Package Description: 30 mL in 1 VIAL, MULTI-DOSE (36987-2006-3)

NDC Information of Mucor plumbeus

NDC Code 36987-2006-3
Proprietary Name Mucor plumbeus
Package Description 30 mL in 1 VIAL, MULTI-DOSE (36987-2006-3)
Product NDC 36987-2006
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Mucor plumbeus
Dosage Form Name INJECTION, SOLUTION
Route Name INTRADERMAL; SUBCUTANEOUS
Start Marketing Date 19720829
Marketing Category Name BLA
Labeler Name Nelco Laboratories, Inc.
Substance Name MUCOR PLUMBEUS
Strength Number .05
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 Mucor plumbeus


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