Alternaria - 49643-101-50 - (Alternaria alternata)

Alphabetical Index


Drug Information of Alternaria

Product NDC: 49643-101
Proprietary Name: Alternaria
Non Proprietary Name: Alternaria alternata
Active Ingredient(s): 1    g/10mL & nbsp;   Alternaria alternata
Administration Route(s): CUTANEOUS; INTRADERMAL; SUBCUTANEOUS
Dosage Form(s): INJECTION
Coding System: National Drug Codes(NDC)

Labeler Information of Alternaria

Product NDC: 49643-101
Labeler Name: Allermed Laboratories, Inc.
Product Type: NON-STANDARDIZED ALLERGENIC
FDA Application Number: BLA102212
Marketing Category: BLA
Start Marketing Date: 19740312

Package Information of Alternaria

Package NDC: 49643-101-50
Package Description: 50 mL in 1 VIAL, MULTI-DOSE (49643-101-50)

NDC Information of Alternaria

NDC Code 49643-101-50
Proprietary Name Alternaria
Package Description 50 mL in 1 VIAL, MULTI-DOSE (49643-101-50)
Product NDC 49643-101
Product Type Name NON-STANDARDIZED ALLERGENIC
Non Proprietary Name Alternaria alternata
Dosage Form Name INJECTION
Route Name CUTANEOUS; INTRADERMAL; SUBCUTANEOUS
Start Marketing Date 19740312
Marketing Category Name BLA
Labeler Name Allermed Laboratories, Inc.
Substance Name ALTERNARIA ALTERNATA
Strength Number 1
Strength Unit g/10mL
Pharmaceutical Classes Non-Standardized Fungal Allergenic Extract [EPC],Increased Histamine Release [PE],Cell-mediated Immunity [PE],Increased IgG Production [PE],Fungal Proteins [Chemical/Ingredient],Allergens [Chemical/Ingredient]

Complete Information of Alternaria


General Information