Home > National Drug Code (NDC) > Whole Bean Cacao

Whole Bean Cacao - 49288-0115-5 - (Whole Bean Cacao)

Alphabetical Index


Drug Information of Whole Bean Cacao

Product NDC: 49288-0115
Proprietary Name: Whole Bean Cacao
Non Proprietary Name: Whole Bean Cacao
Active Ingredient(s): .05    g/mL & nbsp;   Whole Bean Cacao
Administration Route(s): INTRADERMAL; SUBCUTANEOUS
Dosage Form(s): INJECTION, SOLUTION
Coding System: National Drug Codes(NDC)

Labeler Information of Whole Bean Cacao

Product NDC: 49288-0115
Labeler Name: Antigen Laboratories, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: BLA102223
Marketing Category: BLA
Start Marketing Date: 19740323

Package Information of Whole Bean Cacao

Package NDC: 49288-0115-5
Package Description: 50 mL in 1 VIAL, MULTI-DOSE (49288-0115-5)

NDC Information of Whole Bean Cacao

NDC Code 49288-0115-5
Proprietary Name Whole Bean Cacao
Package Description 50 mL in 1 VIAL, MULTI-DOSE (49288-0115-5)
Product NDC 49288-0115
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Whole Bean Cacao
Dosage Form Name INJECTION, SOLUTION
Route Name INTRADERMAL; SUBCUTANEOUS
Start Marketing Date 19740323
Marketing Category Name BLA
Labeler Name Antigen Laboratories, Inc.
Substance Name COCOA BEAN
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],Plant Proteins [Chemical/Ingredient]

Complete Information of Whole Bean Cacao


General Information