Fire Ant - 36987-1778-4 - (Fire Ant)

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Drug Information of Fire Ant

Product NDC: 36987-1778
Proprietary Name: Fire Ant
Non Proprietary Name: Fire Ant
Active Ingredient(s): 10000    [PNU]/mL & nbsp;   Fire Ant
Administration Route(s): INTRADERMAL; SUBCUTANEOUS
Dosage Form(s): INJECTION, SOLUTION
Coding System: National Drug Codes(NDC)

Labeler Information of Fire Ant

Product NDC: 36987-1778
Labeler Name: Nelco Laboratories, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: BLA102192
Marketing Category: BLA
Start Marketing Date: 19720829

Package Information of Fire Ant

Package NDC: 36987-1778-4
Package Description: 50 mL in 1 VIAL, MULTI-DOSE (36987-1778-4)

NDC Information of Fire Ant

NDC Code 36987-1778-4
Proprietary Name Fire Ant
Package Description 50 mL in 1 VIAL, MULTI-DOSE (36987-1778-4)
Product NDC 36987-1778
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Fire Ant
Dosage Form Name INJECTION, SOLUTION
Route Name INTRADERMAL; SUBCUTANEOUS
Start Marketing Date 19720829
Marketing Category Name BLA
Labeler Name Nelco Laboratories, Inc.
Substance Name SOLENOPSIS INVICTA
Strength Number 10000
Strength Unit [PNU]/mL
Pharmaceutical Classes Non-Standardized Insect Venom Allergenic Extract [EPC],Increased Histamine Release [PE],Cell-mediated Immunity [PE],Increased IgG Production [PE],Insect Proteins [Chemical/Ingredient],Ant Venoms [Chemical/Ingredient],Allergens [Chemical/Ingredient]

Complete Information of Fire Ant


General Information