NDC 36987-2214

Flaxseed

Flaxseed

Flaxseed is a Intradermal; Subcutaneous Injection, Solution in the Human Prescription Drug category. It is labeled and distributed by Nelco Laboratories, Inc.. The primary component is Flax Seed.

Product ID36987-2214_f70401b9-9617-41a7-a0c6-ded6f6efa9fa
NDC36987-2214
Product TypeHuman Prescription Drug
Proprietary NameFlaxseed
Generic NameFlaxseed
Dosage FormInjection, Solution
Route of AdministrationINTRADERMAL; SUBCUTANEOUS
Marketing Start Date1972-08-29
Marketing CategoryBLA / BLA
Application NumberBLA102192
Labeler NameNelco Laboratories, Inc.
Substance NameFLAX SEED
Active Ingredient Strength10000 [PNU]/mL
Pharm ClassesNon-Standardized Food Allergenic Extract [EPC],Non-Standardized Plant Allergenic Extract [EPC],Increased Histamine Release [PE],Cell-mediated Immunity [PE],Increased IgG Production [PE],Allergens [CS],Dietary Proteins [CS],Plant Proteins [CS],Seed Storage Proteins [CS]
NDC Exclude FlagE
Listing Certified Through2017-12-31

Packaging

NDC 36987-2214-4

50 mL in 1 VIAL, MULTI-DOSE (36987-2214-4)
Marketing Start Date1972-08-29
NDC Exclude FlagN
Sample Package?N

NDC SPL Data Element Entries

NDC 36987-2214-2 [36987221402]

Flaxseed INJECTION, SOLUTION
Marketing CategoryBLA
Application NumberBLA102192
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date1972-08-29
Inactivation Date2019-10-21

NDC 36987-2214-3 [36987221403]

Flaxseed INJECTION, SOLUTION
Marketing CategoryBLA
Application NumberBLA102192
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date1972-08-29
Inactivation Date2019-10-21

NDC 36987-2214-4 [36987221404]

Flaxseed INJECTION, SOLUTION
Marketing CategoryBLA
Application NumberBLA102192
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date1972-08-29
Inactivation Date2019-10-21

NDC 36987-2214-1 [36987221401]

Flaxseed INJECTION, SOLUTION
Marketing CategoryBLA
Application NumberBLA102192
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date1972-08-29
Inactivation Date2019-10-21

Drug Details

Active Ingredients

IngredientStrength
FLAX SEED10000 [PNU]/mL

OpenFDA Data

SPL SET ID:fb086079-a3f1-458e-8910-2e72c7eae87c
Manufacturer
UNII
RxNorm Concept Unique ID - RxCUI
  • 889596
  • 1014203
  • 901354
  • 904851
  • Pharmacological Class

    • 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 [CS]
    • Dietary Proteins [CS]
    • Plant Proteins [CS]
    • Seed Storage Proteins [CS]

    NDC Crossover Matching brand name "Flaxseed" or generic name "Flaxseed"

    NDCBrand NameGeneric Name
    22840-1521FlaxseedLinum usitatissimum
    22840-1523FlaxseedLinum usitatissimum
    22840-5510FlaxseedLinum usitatissimum
    36987-2214FlaxseedFlaxseed
    36987-2215FlaxseedFlaxseed
    36987-2216FlaxseedFlaxseed
    36987-2217FlaxseedFlaxseed
    36987-2218FlaxseedFlaxseed
    36987-2219FlaxseedFlaxseed
    36987-2220FlaxseedFlaxseed
    36987-2221FlaxseedFlaxseed
    49288-0201FlaxseedFlaxseed
    49643-010FlaxseedFlaxseed

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