NDC 36987-1213

Flounder

Flounder

Flounder 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 Flounder.

Product ID36987-1213_398aea37-e253-4fd4-84ca-ca78367468b5
NDC36987-1213
Product TypeHuman Prescription Drug
Proprietary NameFlounder
Generic NameFlounder
Dosage FormInjection, Solution
Route of AdministrationINTRADERMAL; SUBCUTANEOUS
Marketing Start Date1972-08-29
Marketing CategoryBLA / BLA
Application NumberBLA102192
Labeler NameNelco Laboratories, Inc.
Substance NameFLOUNDER
Active Ingredient Strength0 g/mL
Pharm ClassesNon-Standardized Food Allergenic Extract [EPC],Increased Histamine Release [PE],Cell-mediated Immunity [PE],Allergens [CS],Dietary Proteins [CS],Fish Proteins, Dietary [EXT]
NDC Exclude FlagE
Listing Certified Through2017-12-31

Packaging

NDC 36987-1213-4

50 mL in 1 VIAL, MULTI-DOSE (36987-1213-4)
Marketing Start Date1972-08-29
NDC Exclude FlagN
Sample Package?N

NDC SPL Data Element Entries

NDC 36987-1213-3 [36987121303]

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

NDC 36987-1213-4 [36987121304]

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

NDC 36987-1213-1 [36987121301]

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

NDC 36987-1213-2 [36987121302]

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

Drug Details

Active Ingredients

IngredientStrength
FLOUNDER.1 g/mL

OpenFDA Data

SPL SET ID:026f2f1e-71cf-47ab-a24d-66663ff98429
Manufacturer
UNII
RxNorm Concept Unique ID - RxCUI
  • 905479
  • 892506
  • 905345
  • 892564
  • 904543
  • 901282
  • 892595
  • 892546
  • 966805
  • 899433
  • 966978
  • 901375
  • 904599
  • 901290
  • 899751
  • 899937
  • 905489
  • 901397
  • 905329
  • 892542
  • 905365
  • 892613
  • Pharmacological Class

    • Non-Standardized Food Allergenic Extract [EPC]
    • Increased Histamine Release [PE]
    • Cell-mediated Immunity [PE]
    • Allergens [CS]
    • Dietary Proteins [CS]
    • Fish Proteins
    • Dietary [EXT]

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

    NDCBrand NameGeneric Name
    0268-6137FLOUNDERFlounder
    22840-5771FlounderParalichthys lethostigma
    36987-1210FlounderFlounder
    36987-1211FlounderFlounder
    36987-1212FlounderFlounder
    36987-1213FlounderFlounder
    49288-0200FlounderFlounder
    54575-394FLOUNDERflounder

    Trademark Results [Flounder]

    Mark Image

    Registration | Serial
    Company
    Trademark
    Application Date
    FLOUNDER
    FLOUNDER
    88305255 not registered Live/Pending
    BUZZARDS BAY BREWING, INC.
    2019-02-18
    FLOUNDER
    FLOUNDER
    86078200 not registered Dead/Abandoned
    Buzzards Bay Brewing
    2013-09-30
    FLOUNDER
    FLOUNDER
    78189262 3046736 Dead/Cancelled
    Flounder Motor Homes of California LLC
    2002-11-26
    FLOUNDER
    FLOUNDER
    77019642 3292404 Dead/Cancelled
    Gallimore, Keith
    2006-10-12
    FLOUNDER
    FLOUNDER
    73203052 1140369 Dead/Cancelled
    Universal City Studios, Inc.
    1979-02-07
    FLOUNDER
    FLOUNDER
    73203049 1140411 Dead/Cancelled
    Universal City Studios, Inc.
    1979-02-07
    FLOUNDER
    FLOUNDER
    73203048 1147757 Dead/Cancelled
    Universal City Studios, Inc.
    1979-02-07
    FLOUNDER
    FLOUNDER
    73203047 1140432 Dead/Cancelled
    Universal City Studios, Inc.
    1979-02-07

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