NDC 36987-2416

Cultivated Wheat

Cultivated Wheat

Cultivated Wheat 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 Triticum Aestivum Pollen.

Product ID36987-2416_72e454d7-3ef9-4e04-bd95-d894fab0b155
NDC36987-2416
Product TypeHuman Prescription Drug
Proprietary NameCultivated Wheat
Generic NameCultivated Wheat
Dosage FormInjection, Solution
Route of AdministrationINTRADERMAL; SUBCUTANEOUS
Marketing Start Date1972-08-29
Marketing CategoryBLA / BLA
Application NumberBLA102192
Labeler NameNelco Laboratories, Inc.
Substance NameTRITICUM AESTIVUM 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],Non-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 36987-2416-2

10 mL in 1 VIAL, MULTI-DOSE (36987-2416-2)
Marketing Start Date1972-08-29
NDC Exclude FlagN
Sample Package?N

NDC SPL Data Element Entries

NDC 36987-2416-4 [36987241604]

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

NDC 36987-2416-1 [36987241601]

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

NDC 36987-2416-3 [36987241603]

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

NDC 36987-2416-2 [36987241602]

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

Drug Details

Active Ingredients

IngredientStrength
TRITICUM AESTIVUM POLLEN.05 g/mL

OpenFDA Data

SPL SET ID:f2e3f6a5-ca7d-4f37-bc43-6561da39f9bb
Manufacturer
UNII
RxNorm Concept Unique ID - RxCUI
  • 852332
  • 889573
  • 852200
  • 852139
  • 852676
  • 852346
  • 852117
  • 852662
  • 900151
  • 1014343
  • 852220
  • 852018
  • 1014777
  • 898407
  • 1014734
  • 852700
  • Pharmacological Class

    • Non-Standardized Pollen Allergenic Extract [EPC]
    • Increased Histamine Release [PE]
    • Cell-mediated Immunity [PE]
    • Increased IgG Production [PE]
    • Pollen [CS]
    • Allergens [CS]
    • 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 "Cultivated Wheat" or generic name "Cultivated Wheat"

    NDCBrand NameGeneric Name
    22840-1567Cultivated WheatTriticum aestivum
    22840-1568Cultivated WheatTriticum aestivum
    22840-1587Cultivated WheatTriticum aestivum
    22840-1588Cultivated WheatTriticum aestivum
    22840-1589Cultivated WheatTriticum aestivum
    22840-1590Cultivated WheatTriticum aestivum
    22840-5523Cultivated WheatTriticum aestivum
    36987-2411Cultivated WheatCultivated Wheat
    36987-2412Cultivated WheatCultivated Wheat
    36987-2413Cultivated WheatCultivated Wheat
    36987-2414Cultivated WheatCultivated Wheat
    36987-2415Cultivated WheatCultivated Wheat
    36987-2416Cultivated WheatCultivated Wheat
    36987-2417Cultivated WheatCultivated Wheat
    36987-2418Cultivated WheatCultivated Wheat
    49288-0608Cultivated WheatCultivated Wheat

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