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Kidney Bean - 49288-0061-2 - (Kidney Bean)

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Drug Information of Kidney Bean

Product NDC: 49288-0061
Proprietary Name: Kidney Bean
Non Proprietary Name: Kidney Bean
Active Ingredient(s): .05    g/mL & nbsp;   Kidney Bean
Administration Route(s): INTRADERMAL; SUBCUTANEOUS
Dosage Form(s): INJECTION, SOLUTION
Coding System: National Drug Codes(NDC)

Labeler Information of Kidney Bean

Product NDC: 49288-0061
Labeler Name: Antigen Laboratories, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: BLA102223
Marketing Category: BLA
Start Marketing Date: 19740323

Package Information of Kidney Bean

Package NDC: 49288-0061-2
Package Description: 5 mL in 1 VIAL, MULTI-DOSE (49288-0061-2)

NDC Information of Kidney Bean

NDC Code 49288-0061-2
Proprietary Name Kidney Bean
Package Description 5 mL in 1 VIAL, MULTI-DOSE (49288-0061-2)
Product NDC 49288-0061
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Kidney Bean
Dosage Form Name INJECTION, SOLUTION
Route Name INTRADERMAL; SUBCUTANEOUS
Start Marketing Date 19740323
Marketing Category Name BLA
Labeler Name Antigen Laboratories, Inc.
Substance Name KIDNEY BEAN
Strength Number .05
Strength Unit g/mL
Pharmaceutical Classes Non-Standardized Plant Allergenic Extract [EPC],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],Vegetable Proteins [Chemical/Ingredient]

Complete Information of Kidney Bean


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