Hackberry - 36987-3351-4 - (Hackberry)

Alphabetical Index


Drug Information of Hackberry

Product NDC: 36987-3351
Proprietary Name: Hackberry
Non Proprietary Name: Hackberry
Active Ingredient(s): 20000    [PNU]/mL & nbsp;   Hackberry
Administration Route(s): INTRADERMAL; SUBCUTANEOUS
Dosage Form(s): INJECTION, SOLUTION
Coding System: National Drug Codes(NDC)

Labeler Information of Hackberry

Product NDC: 36987-3351
Labeler Name: Nelco Laboratories, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: BLA102192
Marketing Category: BLA
Start Marketing Date: 19720829

Package Information of Hackberry

Package NDC: 36987-3351-4
Package Description: 50 mL in 1 VIAL, MULTI-DOSE (36987-3351-4)

NDC Information of Hackberry

NDC Code 36987-3351-4
Proprietary Name Hackberry
Package Description 50 mL in 1 VIAL, MULTI-DOSE (36987-3351-4)
Product NDC 36987-3351
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Hackberry
Dosage Form Name INJECTION, SOLUTION
Route Name INTRADERMAL; SUBCUTANEOUS
Start Marketing Date 19720829
Marketing Category Name BLA
Labeler Name Nelco Laboratories, Inc.
Substance Name CELTIS OCCIDENTALIS POLLEN
Strength Number 20000
Strength Unit [PNU]/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 Hackberry


General Information