Flaxseed - 36987-2217-3 - (Flaxseed)

Alphabetical Index


Drug Information of Flaxseed

Product NDC: 36987-2217
Proprietary Name: Flaxseed
Non Proprietary Name: Flaxseed
Active Ingredient(s): 20000    [PNU]/mL & nbsp;   Flaxseed
Administration Route(s): INTRADERMAL; SUBCUTANEOUS
Dosage Form(s): INJECTION, SOLUTION
Coding System: National Drug Codes(NDC)

Labeler Information of Flaxseed

Product NDC: 36987-2217
Labeler Name: Nelco Laboratories, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: BLA102192
Marketing Category: BLA
Start Marketing Date: 19720829

Package Information of Flaxseed

Package NDC: 36987-2217-3
Package Description: 30 mL in 1 VIAL, MULTI-DOSE (36987-2217-3)

NDC Information of Flaxseed

NDC Code 36987-2217-3
Proprietary Name Flaxseed
Package Description 30 mL in 1 VIAL, MULTI-DOSE (36987-2217-3)
Product NDC 36987-2217
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Flaxseed
Dosage Form Name INJECTION, SOLUTION
Route Name INTRADERMAL; SUBCUTANEOUS
Start Marketing Date 19720829
Marketing Category Name BLA
Labeler Name Nelco Laboratories, Inc.
Substance Name FLAX SEED
Strength Number 20000
Strength Unit [PNU]/mL
Pharmaceutical Classes Non-Standardized Food Allergenic Extract [EPC],Non-Standardized Plant Allergenic Extract [EPC],Increased Histamine Release [PE],Cell-mediated Immunity [PE],Increased IgG Production [PE],Allergens [Chemical/Ingredient],Dietary Proteins [Chemical/Ingredient],Plant Proteins [Chemical/Ingredient],Seed Storage Proteins [Chemical/Ingredient]

Complete Information of Flaxseed


General Information