NDC 36987-2220

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 ID36987-2220_3f71b69c-37b8-4c27-af1a-cc5178f3ff61
NDC36987-2220
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 Strength0 g/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 36987-2220-1

5 mL in 1 VIAL, MULTI-DOSE (36987-2220-1)
Marketing Start Date1972-08-29
NDC Exclude FlagN
Sample Package?N

NDC SPL Data Element Entries

NDC 36987-2220-4 [36987222004]

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

NDC 36987-2220-1 [36987222001]

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

NDC 36987-2220-2 [36987222002]

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

NDC 36987-2220-3 [36987222003]

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 SEED.1 g/mL

OpenFDA Data

SPL SET ID:9a0a10e2-1458-4e1a-a678-2a3863f22f5a
Manufacturer
UNII
RxNorm Concept Unique ID - RxCUI
  • 851885
  • 966930
  • 904971
  • 852415
  • 852318
  • 889600
  • 904638
  • 966962
  • 852547
  • 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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