ACACIA - 0268-6676-05 - (Acacia)

Alphabetical Index


Drug Information of ACACIA

Product NDC: 0268-6676
Proprietary Name: ACACIA
Non Proprietary Name: Acacia
Active Ingredient(s): 1000    [PNU]/mL & nbsp;   Acacia
Administration Route(s): INTRADERMAL
Dosage Form(s): INJECTION, SOLUTION
Coding System: National Drug Codes(NDC)

Labeler Information of ACACIA

Product NDC: 0268-6676
Labeler Name: ALK-Abello, Inc.
Product Type: NON-STANDARDIZED ALLERGENIC
FDA Application Number: BLA103753
Marketing Category: BLA
Start Marketing Date: 19650101

Package Information of ACACIA

Package NDC: 0268-6676-05
Package Description: 5 mL in 1 VIAL, MULTI-DOSE (0268-6676-05)

NDC Information of ACACIA

NDC Code 0268-6676-05
Proprietary Name ACACIA
Package Description 5 mL in 1 VIAL, MULTI-DOSE (0268-6676-05)
Product NDC 0268-6676
Product Type Name NON-STANDARDIZED ALLERGENIC
Non Proprietary Name Acacia
Dosage Form Name INJECTION, SOLUTION
Route Name INTRADERMAL
Start Marketing Date 19650101
Marketing Category Name BLA
Labeler Name ALK-Abello, Inc.
Substance Name ACACIA
Strength Number 1000
Strength Unit [PNU]/mL
Pharmaceutical Classes Non-Standardized Plant Allergenic Extract [EPC],Increased Histamine Release [PE],Cell-mediated Immunity [PE],Increased IgG Production [PE],Plant Proteins [Chemical/Ingredient],Allergens [Chemical/Ingredient]

Complete Information of ACACIA


General Information