NDC 36987-2735

Black Locust

Black Locust

Black Locust 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 Robinia Pseudoacacia Pollen.

Product ID36987-2735_90c4b6c4-a7f2-4ba8-927c-8440e0df96f5
NDC36987-2735
Product TypeHuman Prescription Drug
Proprietary NameBlack Locust
Generic NameBlack Locust
Dosage FormInjection, Solution
Route of AdministrationINTRADERMAL; SUBCUTANEOUS
Marketing Start Date1972-08-29
Marketing CategoryBLA / BLA
Application NumberBLA102192
Labeler NameNelco Laboratories, Inc.
Substance NameROBINIA PSEUDOACACIA POLLEN
Active Ingredient Strength20000 [PNU]/mL
Pharm ClassesNon-Standardized Pollen Allergenic Extract [EPC],Increased Histamine Release [PE],Cell-mediated Immunity [PE],Increased IgG Production [PE],Pollen [CS],Allergens [CS]
NDC Exclude FlagE
Listing Certified Through2017-12-31

Packaging

NDC 36987-2735-2

10 mL in 1 VIAL, MULTI-DOSE (36987-2735-2)
Marketing Start Date1972-08-29
NDC Exclude FlagN
Sample Package?N

NDC SPL Data Element Entries

NDC 36987-2735-3 [36987273503]

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

NDC 36987-2735-1 [36987273501]

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

NDC 36987-2735-4 [36987273504]

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

NDC 36987-2735-2 [36987273502]

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

Drug Details

Active Ingredients

IngredientStrength
ROBINIA PSEUDOACACIA POLLEN20000 [PNU]/mL

OpenFDA Data

SPL SET ID:de47ad70-b2be-4103-a402-35463ebffc87
Manufacturer
UNII
RxNorm Concept Unique ID - RxCUI
  • 1014335
  • 1044512
  • 889558
  • 1014689
  • 1043789
  • 900896
  • 1014684
  • 895362
  • 1044339
  • 1013902
  • 1013927
  • 895685
  • 1014357
  • 900940
  • 1044387
  • 898422
  • 899570
  • 883499
  • 1014718
  • 900074
  • 1013887
  • 1014311
  • 1044400
  • 1013880
  • 1013873
  • 1013869
  • 900030
  • 889630
  • 899602
  • 895449
  • 1044490
  • 899686
  • 1013951
  • 1044355
  • 1044347
  • 899968
  • 1013959
  • 1044213
  • 1044486
  • 1043795
  • 899960
  • 900957
  • 1044357
  • 895378
  • 1014699
  • 1044316
  • 1300000
  • 1014324
  • 1014771
  • 1014222
  • 1006476
  • 1013910
  • 895694
  • 1044300
  • 1043685
  • 900040
  • 899561
  • 899634
  • 899588
  • 1014268
  • 900088
  • 1232595
  • 1044224
  • 899779
  • 900720
  • 1044320
  • 895602
  • 1232570
  • 895708
  • 1044230
  • 1115278
  • 889642
  • 900740
  • 895474
  • 1044519
  • 1013942
  • 899678
  • 1044327
  • 1013968
  • 900056
  • 900120
  • 899698
  • 901031
  • 899984
  • Pharmacological Class

    • Non-Standardized Pollen Allergenic Extract [EPC]
    • Increased Histamine Release [PE]
    • Cell-mediated Immunity [PE]
    • Increased IgG Production [PE]
    • Pollen [CS]
    • Allergens [CS]

    NDC Crossover Matching brand name "Black Locust" or generic name "Black Locust"

    NDCBrand NameGeneric Name
    36987-2733Black LocustBlack Locust
    36987-2734Black LocustBlack Locust
    36987-2735Black LocustBlack Locust
    36987-2736Black LocustBlack Locust
    36987-2737Black LocustBlack Locust
    36987-2738Black LocustBlack Locust
    36987-2739Black LocustBlack Locust
    36987-2740Black LocustBlack Locust
    62106-8775ROBINIA PSEUDOACACIABlack locust
    0268-6722ROBINIA PSEUDOACACIA POLLENBlack Locust
    0268-6723ROBINIA PSEUDOACACIA POLLENBlack Locust

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