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Stemphylium sarciniforms - 36987-2114-3 - (Stemphylium sarciniforms)

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Drug Information of Stemphylium sarciniforms

Product NDC: 36987-2114
Proprietary Name: Stemphylium sarciniforms
Non Proprietary Name: Stemphylium sarciniforms
Active Ingredient(s): .05    g/mL & nbsp;   Stemphylium sarciniforms
Administration Route(s): INTRADERMAL; SUBCUTANEOUS
Dosage Form(s): INJECTION, SOLUTION
Coding System: National Drug Codes(NDC)

Labeler Information of Stemphylium sarciniforms

Product NDC: 36987-2114
Labeler Name: Nelco Laboratories, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: BLA102192
Marketing Category: BLA
Start Marketing Date: 19720829

Package Information of Stemphylium sarciniforms

Package NDC: 36987-2114-3
Package Description: 30 mL in 1 VIAL, MULTI-DOSE (36987-2114-3)

NDC Information of Stemphylium sarciniforms

NDC Code 36987-2114-3
Proprietary Name Stemphylium sarciniforms
Package Description 30 mL in 1 VIAL, MULTI-DOSE (36987-2114-3)
Product NDC 36987-2114
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Stemphylium sarciniforms
Dosage Form Name INJECTION, SOLUTION
Route Name INTRADERMAL; SUBCUTANEOUS
Start Marketing Date 19720829
Marketing Category Name BLA
Labeler Name Nelco Laboratories, Inc.
Substance Name STEMPHYLIUM SARCINIFORME
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 Stemphylium sarciniforms


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