Hackberry - 49288-0260-3 - (Hackberry)

Alphabetical Index


Drug Information of Hackberry

Product NDC: 49288-0260
Proprietary Name: Hackberry
Non Proprietary Name: Hackberry
Active Ingredient(s): .05    g/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: 49288-0260
Labeler Name: Antigen Laboratories, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: BLA102223
Marketing Category: BLA
Start Marketing Date: 19740323

Package Information of Hackberry

Package NDC: 49288-0260-3
Package Description: 10 mL in 1 VIAL, MULTI-DOSE (49288-0260-3)

NDC Information of Hackberry

NDC Code 49288-0260-3
Proprietary Name Hackberry
Package Description 10 mL in 1 VIAL, MULTI-DOSE (49288-0260-3)
Product NDC 49288-0260
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Hackberry
Dosage Form Name INJECTION, SOLUTION
Route Name INTRADERMAL; SUBCUTANEOUS
Start Marketing Date 19740323
Marketing Category Name BLA
Labeler Name Antigen Laboratories, Inc.
Substance Name CELTIS OCCIDENTALIS 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 Hackberry


General Information