Home > National Drug Code (NDC) > Arizona Cypress

Arizona Cypress - 36987-2620-2 - (Arizona Cypress)

Alphabetical Index


Drug Information of Arizona Cypress

Product NDC: 36987-2620
Proprietary Name: Arizona Cypress
Non Proprietary Name: Arizona Cypress
Active Ingredient(s): .1    g/mL & nbsp;   Arizona Cypress
Administration Route(s): INTRADERMAL; SUBCUTANEOUS
Dosage Form(s): INJECTION, SOLUTION
Coding System: National Drug Codes(NDC)

Labeler Information of Arizona Cypress

Product NDC: 36987-2620
Labeler Name: Nelco Laboratories, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: BLA102192
Marketing Category: BLA
Start Marketing Date: 19720829

Package Information of Arizona Cypress

Package NDC: 36987-2620-2
Package Description: 10 mL in 1 VIAL, MULTI-DOSE (36987-2620-2)

NDC Information of Arizona Cypress

NDC Code 36987-2620-2
Proprietary Name Arizona Cypress
Package Description 10 mL in 1 VIAL, MULTI-DOSE (36987-2620-2)
Product NDC 36987-2620
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Arizona Cypress
Dosage Form Name INJECTION, SOLUTION
Route Name INTRADERMAL; SUBCUTANEOUS
Start Marketing Date 19720829
Marketing Category Name BLA
Labeler Name Nelco Laboratories, Inc.
Substance Name CUPRESSUS ARIZONICA POLLEN
Strength Number .1
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 Arizona Cypress


General Information