Sisal - 49643-021-10 - (Sisal)

Alphabetical Index


Drug Information of Sisal

Product NDC: 49643-021
Proprietary Name: Sisal
Non Proprietary Name: Sisal
Active Ingredient(s): 1    g/10mL & nbsp;   Sisal
Administration Route(s): CUTANEOUS; INTRADERMAL; SUBCUTANEOUS
Dosage Form(s): INJECTION
Coding System: National Drug Codes(NDC)

Labeler Information of Sisal

Product NDC: 49643-021
Labeler Name: Allermed Laboratories, Inc.
Product Type: NON-STANDARDIZED ALLERGENIC
FDA Application Number: BLA102212
Marketing Category: BLA
Start Marketing Date: 19740312

Package Information of Sisal

Package NDC: 49643-021-10
Package Description: 10 mL in 1 VIAL, MULTI-DOSE (49643-021-10)

NDC Information of Sisal

NDC Code 49643-021-10
Proprietary Name Sisal
Package Description 10 mL in 1 VIAL, MULTI-DOSE (49643-021-10)
Product NDC 49643-021
Product Type Name NON-STANDARDIZED ALLERGENIC
Non Proprietary Name Sisal
Dosage Form Name INJECTION
Route Name CUTANEOUS; INTRADERMAL; SUBCUTANEOUS
Start Marketing Date 19740312
Marketing Category Name BLA
Labeler Name Allermed Laboratories, Inc.
Substance Name AGAVE SISALANA FIBER
Strength Number 1
Strength Unit g/10mL
Pharmaceutical Classes Non-Standardized Plant Fiber 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 Sisal


General Information