Beet - 49288-0052-4 - (Beet)

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Drug Information of Beet

Product NDC: 49288-0052
Proprietary Name: Beet
Non Proprietary Name: Beet
Active Ingredient(s): .05    g/mL & nbsp;   Beet
Administration Route(s): INTRADERMAL; SUBCUTANEOUS
Dosage Form(s): INJECTION, SOLUTION
Coding System: National Drug Codes(NDC)

Labeler Information of Beet

Product NDC: 49288-0052
Labeler Name: Antigen Laboratories, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: BLA102223
Marketing Category: BLA
Start Marketing Date: 19740323

Package Information of Beet

Package NDC: 49288-0052-4
Package Description: 30 mL in 1 VIAL, MULTI-DOSE (49288-0052-4)

NDC Information of Beet

NDC Code 49288-0052-4
Proprietary Name Beet
Package Description 30 mL in 1 VIAL, MULTI-DOSE (49288-0052-4)
Product NDC 49288-0052
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Beet
Dosage Form Name INJECTION, SOLUTION
Route Name INTRADERMAL; SUBCUTANEOUS
Start Marketing Date 19740323
Marketing Category Name BLA
Labeler Name Antigen Laboratories, Inc.
Substance Name BEET
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 Beet


General Information