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Botrytis cinerea - 36987-1904-1 - (Botrytis cinerea)

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Drug Information of Botrytis cinerea

Product NDC: 36987-1904
Proprietary Name: Botrytis cinerea
Non Proprietary Name: Botrytis cinerea
Active Ingredient(s): 20000    [PNU]/mL & nbsp;   Botrytis cinerea
Administration Route(s): INTRADERMAL; SUBCUTANEOUS
Dosage Form(s): INJECTION, SOLUTION
Coding System: National Drug Codes(NDC)

Labeler Information of Botrytis cinerea

Product NDC: 36987-1904
Labeler Name: Nelco Laboratories, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: BLA102192
Marketing Category: BLA
Start Marketing Date: 19720829

Package Information of Botrytis cinerea

Package NDC: 36987-1904-1
Package Description: 5 mL in 1 VIAL, MULTI-DOSE (36987-1904-1)

NDC Information of Botrytis cinerea

NDC Code 36987-1904-1
Proprietary Name Botrytis cinerea
Package Description 5 mL in 1 VIAL, MULTI-DOSE (36987-1904-1)
Product NDC 36987-1904
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Botrytis cinerea
Dosage Form Name INJECTION, SOLUTION
Route Name INTRADERMAL; SUBCUTANEOUS
Start Marketing Date 19720829
Marketing Category Name BLA
Labeler Name Nelco Laboratories, Inc.
Substance Name BOTRYTIS CINEREA
Strength Number 20000
Strength Unit [PNU]/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 Botrytis cinerea


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