NDC 36987-3012

Lombardy Poplar

Lombardy Poplar

Lombardy Poplar 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 Populus Nigra Pollen.

Product ID36987-3012_69cd05e6-a993-428b-9b0c-0235126ba63b
NDC36987-3012
Product TypeHuman Prescription Drug
Proprietary NameLombardy Poplar
Generic NameLombardy Poplar
Dosage FormInjection, Solution
Route of AdministrationINTRADERMAL; SUBCUTANEOUS
Marketing Start Date1972-08-29
Marketing CategoryBLA / BLA
Application NumberBLA102192
Labeler NameNelco Laboratories, Inc.
Substance NamePOPULUS NIGRA POLLEN
Active Ingredient Strength0 g/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 36987-3012-1

5 mL in 1 VIAL, MULTI-DOSE (36987-3012-1)
Marketing Start Date1972-08-29
NDC Exclude FlagN
Sample Package?N

NDC SPL Data Element Entries

NDC 36987-3012-2 [36987301202]

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

NDC 36987-3012-3 [36987301203]

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

NDC 36987-3012-1 [36987301201]

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

NDC 36987-3012-4 [36987301204]

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

Drug Details

Active Ingredients

IngredientStrength
POPULUS NIGRA POLLEN.1 g/mL

OpenFDA Data

SPL SET ID:573781d0-e50e-42ff-8a46-2292b8107ce7
Manufacturer
UNII
RxNorm Concept Unique ID - RxCUI
  • 900922
  • 897982
  • 895689
  • 1044515
  • 897984
  • 1044305
  • 895683
  • 1013923
  • 1043785
  • 1014680
  • 900052
  • 899980
  • 900763
  • 1014230
  • 1044472
  • 899598
  • 900716
  • 1044341
  • 883495
  • 901500
  • 900736
  • 1115271
  • 895445
  • 883416
  • 1044331
  • 901021
  • 1014442
  • 1044298
  • 889636
  • 1044488
  • 899555
  • 900799
  • 898024
  • 899684
  • 900095
  • 1014328
  • 1013883
  • 897408
  • 901027
  • 895461
  • 895358
  • 898002
  • 968772
  • 1006376
  • 1013955
  • 1044510
  • 1044261
  • 1044322
  • 1044353
  • 1014687
  • 900950
  • 900885
  • 895370
  • 1115837
  • 1043791
  • 1044359
  • 1012218
  • 1044390
  • 900024
  • 1044396
  • 899566
  • 897361
  • 1044226
  • 895598
  • 900976
  • 899581
  • 900066
  • 1044220
  • 1013891
  • 899964
  • 1014235
  • 883406
  • 1044351
  • 889648
  • 899616
  • 895704
  • 900085
  • 899694
  • 1044207
  • 1299994
  • 900749
  • 900843
  • 899958
  • 1232565
  • 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 "Lombardy Poplar" or generic name "Lombardy Poplar"

    NDCBrand NameGeneric Name
    36987-3005Lombardy PoplarLombardy Poplar
    36987-3006Lombardy PoplarLombardy Poplar
    36987-3007Lombardy PoplarLombardy Poplar
    36987-3008Lombardy PoplarLombardy Poplar
    36987-3009Lombardy PoplarLombardy Poplar
    36987-3010Lombardy PoplarLombardy Poplar
    36987-3011Lombardy PoplarLombardy Poplar
    36987-3012Lombardy PoplarLombardy Poplar
    49288-0419Lombardy PoplarLombardy Poplar

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