Home > National Drug Code (NDC) > ALTERNARIA TENUIS ALTERNATA

ALTERNARIA TENUIS ALTERNATA - 54575-181-10 - (alternaria alternata)

Alphabetical Index


Drug Information of ALTERNARIA TENUIS ALTERNATA

Product NDC: 54575-181
Proprietary Name: ALTERNARIA TENUIS ALTERNATA
Non Proprietary Name: alternaria alternata
Active Ingredient(s): 1    g/20mL & nbsp;   alternaria alternata
Administration Route(s): PERCUTANEOUS; SUBCUTANEOUS
Dosage Form(s): INJECTION, SOLUTION
Coding System: National Drug Codes(NDC)

Labeler Information of ALTERNARIA TENUIS ALTERNATA

Product NDC: 54575-181
Labeler Name: Allergy Laboratories, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: BLA101376
Marketing Category: BLA
Start Marketing Date: 19671207

Package Information of ALTERNARIA TENUIS ALTERNATA

Package NDC: 54575-181-10
Package Description: 10 mL in 1 VIAL, MULTI-DOSE (54575-181-10)

NDC Information of ALTERNARIA TENUIS ALTERNATA

NDC Code 54575-181-10
Proprietary Name ALTERNARIA TENUIS ALTERNATA
Package Description 10 mL in 1 VIAL, MULTI-DOSE (54575-181-10)
Product NDC 54575-181
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name alternaria alternata
Dosage Form Name INJECTION, SOLUTION
Route Name PERCUTANEOUS; SUBCUTANEOUS
Start Marketing Date 19671207
Marketing Category Name BLA
Labeler Name Allergy Laboratories, Inc.
Substance Name ALTERNARIA ALTERNATA
Strength Number 1
Strength Unit g/20mL
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 TENUIS ALTERNATA


General Information