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Sunflower Seed - 49288-0483-5 - (Sunflower Seed)

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Drug Information of Sunflower Seed

Product NDC: 49288-0483
Proprietary Name: Sunflower Seed
Non Proprietary Name: Sunflower Seed
Active Ingredient(s): .05    g/mL & nbsp;   Sunflower Seed
Administration Route(s): INTRADERMAL; SUBCUTANEOUS
Dosage Form(s): INJECTION, SOLUTION
Coding System: National Drug Codes(NDC)

Labeler Information of Sunflower Seed

Product NDC: 49288-0483
Labeler Name: Antigen Laboratories, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: BLA102223
Marketing Category: BLA
Start Marketing Date: 19740323

Package Information of Sunflower Seed

Package NDC: 49288-0483-5
Package Description: 50 mL in 1 VIAL, MULTI-DOSE (49288-0483-5)

NDC Information of Sunflower Seed

NDC Code 49288-0483-5
Proprietary Name Sunflower Seed
Package Description 50 mL in 1 VIAL, MULTI-DOSE (49288-0483-5)
Product NDC 49288-0483
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Sunflower Seed
Dosage Form Name INJECTION, SOLUTION
Route Name INTRADERMAL; SUBCUTANEOUS
Start Marketing Date 19740323
Marketing Category Name BLA
Labeler Name Antigen Laboratories, Inc.
Substance Name SUNFLOWER SEED
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],Seed Storage Proteins [Chemical/Ingredient],Plant Proteins [Chemical/Ingredient]

Complete Information of Sunflower Seed


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