SILK - 54575-278-02 - (bombyx mori fiber)

Alphabetical Index


Drug Information of SILK

Product NDC: 54575-278
Proprietary Name: SILK
Non Proprietary Name: bombyx mori fiber
Active Ingredient(s): 1    g/20mL & nbsp;   bombyx mori fiber
Administration Route(s): PERCUTANEOUS; SUBCUTANEOUS
Dosage Form(s): INJECTION, SOLUTION
Coding System: National Drug Codes(NDC)

Labeler Information of SILK

Product NDC: 54575-278
Labeler Name: Allergy Laboratories, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: BLA101376
Marketing Category: BLA
Start Marketing Date: 19671207

Package Information of SILK

Package NDC: 54575-278-02
Package Description: 2 mL in 1 VIAL, MULTI-DOSE (54575-278-02)

NDC Information of SILK

NDC Code 54575-278-02
Proprietary Name SILK
Package Description 2 mL in 1 VIAL, MULTI-DOSE (54575-278-02)
Product NDC 54575-278
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name bombyx mori fiber
Dosage Form Name INJECTION, SOLUTION
Route Name PERCUTANEOUS; SUBCUTANEOUS
Start Marketing Date 19671207
Marketing Category Name BLA
Labeler Name Allergy Laboratories, Inc.
Substance Name BOMBYX MORI FIBER
Strength Number 1
Strength Unit g/20mL
Pharmaceutical Classes Non-Standardized Insect Allergenic Extract [EPC],Increased Histamine Release [PE],Cell-mediated Immunity [PE],Increased IgG Production [PE],Insect Proteins [Chemical/Ingredient],Silk [Chemical/Ingredient],Allergens [Chemical/Ingredient]

Complete Information of SILK


General Information