Ailanthus - 36987-3362-2 - (Ailanthus)

Alphabetical Index


Drug Information of Ailanthus

Product NDC: 36987-3362
Proprietary Name: Ailanthus
Non Proprietary Name: Ailanthus
Active Ingredient(s): .05    g/mL & nbsp;   Ailanthus
Administration Route(s): INTRADERMAL; SUBCUTANEOUS
Dosage Form(s): INJECTION, SOLUTION
Coding System: National Drug Codes(NDC)

Labeler Information of Ailanthus

Product NDC: 36987-3362
Labeler Name: Nelco Laboratories, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: BLA102192
Marketing Category: BLA
Start Marketing Date: 19720829

Package Information of Ailanthus

Package NDC: 36987-3362-2
Package Description: 10 mL in 1 VIAL, MULTI-DOSE (36987-3362-2)

NDC Information of Ailanthus

NDC Code 36987-3362-2
Proprietary Name Ailanthus
Package Description 10 mL in 1 VIAL, MULTI-DOSE (36987-3362-2)
Product NDC 36987-3362
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Ailanthus
Dosage Form Name INJECTION, SOLUTION
Route Name INTRADERMAL; SUBCUTANEOUS
Start Marketing Date 19720829
Marketing Category Name BLA
Labeler Name Nelco Laboratories, Inc.
Substance Name AILANTHUS ALTISSIMA POLLEN
Strength Number .05
Strength Unit g/mL
Pharmaceutical Classes Non-Standardized Pollen Allergenic Extract [EPC],Increased Histamine Release [PE],Cell-mediated Immunity [PE],Increased IgG Production [PE],Pollen [Chemical/Ingredient],Allergens [Chemical/Ingredient]

Complete Information of Ailanthus


General Information