Sole - 49288-0473-5 - (Sole)

Alphabetical Index


Drug Information of Sole

Product NDC: 49288-0473
Proprietary Name: Sole
Non Proprietary Name: Sole
Active Ingredient(s): .05    g/mL & nbsp;   Sole
Administration Route(s): INTRADERMAL; SUBCUTANEOUS
Dosage Form(s): INJECTION, SOLUTION
Coding System: National Drug Codes(NDC)

Labeler Information of Sole

Product NDC: 49288-0473
Labeler Name: Antigen Laboratories, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: BLA102223
Marketing Category: BLA
Start Marketing Date: 19740323

Package Information of Sole

Package NDC: 49288-0473-5
Package Description: 50 mL in 1 VIAL, MULTI-DOSE (49288-0473-5)

NDC Information of Sole

NDC Code 49288-0473-5
Proprietary Name Sole
Package Description 50 mL in 1 VIAL, MULTI-DOSE (49288-0473-5)
Product NDC 49288-0473
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Sole
Dosage Form Name INJECTION, SOLUTION
Route Name INTRADERMAL; SUBCUTANEOUS
Start Marketing Date 19740323
Marketing Category Name BLA
Labeler Name Antigen Laboratories, Inc.
Substance Name ENGLISH SOLE
Strength Number .05
Strength Unit g/mL
Pharmaceutical Classes Non-Standardized Food Allergenic Extract [EPC],Increased Histamine Release [PE],Cell-mediated Immunity [PE],Allergens [Chemical/Ingredient],Dietary Proteins [Chemical/Ingredient],Fish Proteins, Dietary [Chemical/Ingredient]

Complete Information of Sole


General Information