Mosquito - 36987-1812-3 - (Mosquito)

Alphabetical Index


Drug Information of Mosquito

Product NDC: 36987-1812
Proprietary Name: Mosquito
Non Proprietary Name: Mosquito
Active Ingredient(s): 10000    [PNU]/mL & nbsp;   Mosquito
Administration Route(s): INTRADERMAL; SUBCUTANEOUS
Dosage Form(s): INJECTION, SOLUTION
Coding System: National Drug Codes(NDC)

Labeler Information of Mosquito

Product NDC: 36987-1812
Labeler Name: Nelco Laboratories, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: BLA102192
Marketing Category: BLA
Start Marketing Date: 19720829

Package Information of Mosquito

Package NDC: 36987-1812-3
Package Description: 30 mL in 1 VIAL, MULTI-DOSE (36987-1812-3)

NDC Information of Mosquito

NDC Code 36987-1812-3
Proprietary Name Mosquito
Package Description 30 mL in 1 VIAL, MULTI-DOSE (36987-1812-3)
Product NDC 36987-1812
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Mosquito
Dosage Form Name INJECTION, SOLUTION
Route Name INTRADERMAL; SUBCUTANEOUS
Start Marketing Date 19720829
Marketing Category Name BLA
Labeler Name Nelco Laboratories, Inc.
Substance Name AEDES TAENIORHYNCHUS
Strength Number 10000
Strength Unit [PNU]/mL
Pharmaceutical Classes Non-Standardized Insect Allergenic Extract [EPC],Increased Histamine Release [PE],Cell-mediated Immunity [PE],Increased IgG Production [PE],Insect Proteins [Chemical/Ingredient],Allergens [Chemical/Ingredient]

Complete Information of Mosquito


General Information