Buckwheat - 49288-0051-1 - (Buckwheat)

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Drug Information of Buckwheat

Product NDC: 49288-0051
Proprietary Name: Buckwheat
Non Proprietary Name: Buckwheat
Active Ingredient(s): .05    g/mL & nbsp;   Buckwheat
Administration Route(s): INTRADERMAL; SUBCUTANEOUS
Dosage Form(s): INJECTION, SOLUTION
Coding System: National Drug Codes(NDC)

Labeler Information of Buckwheat

Product NDC: 49288-0051
Labeler Name: Antigen Laboratories, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: BLA102223
Marketing Category: BLA
Start Marketing Date: 19740323

Package Information of Buckwheat

Package NDC: 49288-0051-1
Package Description: 2 mL in 1 VIAL, MULTI-DOSE (49288-0051-1)

NDC Information of Buckwheat

NDC Code 49288-0051-1
Proprietary Name Buckwheat
Package Description 2 mL in 1 VIAL, MULTI-DOSE (49288-0051-1)
Product NDC 49288-0051
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Buckwheat
Dosage Form Name INJECTION, SOLUTION
Route Name INTRADERMAL; SUBCUTANEOUS
Start Marketing Date 19740323
Marketing Category Name BLA
Labeler Name Antigen Laboratories, Inc.
Substance Name BUCKWHEAT
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],Grain Proteins [Chemical/Ingredient]

Complete Information of Buckwheat


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