White Ash - 49288-0021-4 - (White Ash)

Alphabetical Index


Drug Information of White Ash

Product NDC: 49288-0021
Proprietary Name: White Ash
Non Proprietary Name: White Ash
Active Ingredient(s): .1    g/mL & nbsp;   White Ash
Administration Route(s): INTRADERMAL; SUBCUTANEOUS
Dosage Form(s): INJECTION, SOLUTION
Coding System: National Drug Codes(NDC)

Labeler Information of White Ash

Product NDC: 49288-0021
Labeler Name: Antigen Laboratories, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: BLA102223
Marketing Category: BLA
Start Marketing Date: 19920413

Package Information of White Ash

Package NDC: 49288-0021-4
Package Description: 30 mL in 1 VIAL, MULTI-DOSE (49288-0021-4)

NDC Information of White Ash

NDC Code 49288-0021-4
Proprietary Name White Ash
Package Description 30 mL in 1 VIAL, MULTI-DOSE (49288-0021-4)
Product NDC 49288-0021
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name White Ash
Dosage Form Name INJECTION, SOLUTION
Route Name INTRADERMAL; SUBCUTANEOUS
Start Marketing Date 19920413
Marketing Category Name BLA
Labeler Name Antigen Laboratories, Inc.
Substance Name FRAXINUS AMERICANA 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 White Ash


General Information