NDC 36987-2375

Giant Wild Rye

Giant Wild Rye

Giant Wild Rye 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 Leymus Condensatus Pollen.

Product ID36987-2375_467064a9-eca5-4b65-bdbb-0323fb27bcf6
NDC36987-2375
Product TypeHuman Prescription Drug
Proprietary NameGiant Wild Rye
Generic NameGiant Wild Rye
Dosage FormInjection, Solution
Route of AdministrationINTRADERMAL; SUBCUTANEOUS
Marketing Start Date1972-08-29
Marketing CategoryBLA / BLA
Application NumberBLA102192
Labeler NameNelco Laboratories, Inc.
Substance NameLEYMUS CONDENSATUS 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 36987-2375-4

50 mL in 1 VIAL, MULTI-DOSE (36987-2375-4)
Marketing Start Date1972-08-29
NDC Exclude FlagN
Sample Package?N

NDC SPL Data Element Entries

NDC 36987-2375-2 [36987237502]

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

NDC 36987-2375-4 [36987237504]

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

NDC 36987-2375-3 [36987237503]

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

NDC 36987-2375-1 [36987237501]

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

Drug Details

Active Ingredients

IngredientStrength
LEYMUS CONDENSATUS POLLEN20000 [PNU]/mL

OpenFDA Data

SPL SET ID:394c5437-08b9-49ae-a90c-2c5d5b449344
Manufacturer
UNII
RxNorm Concept Unique ID - RxCUI
  • 889666
  • 897359
  • 899541
  • 889565
  • 900012
  • 897351
  • 898409
  • 1014347
  • 899976
  • 900161
  • 898136
  • 1044242
  • 1013966
  • 889530
  • 1044526
  • 1044504
  • 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 "Giant Wild Rye" or generic name "Giant Wild Rye"

    NDCBrand NameGeneric Name
    36987-2373Giant Wild RyeGiant Wild Rye
    36987-2374Giant Wild RyeGiant Wild Rye
    36987-2375Giant Wild RyeGiant Wild Rye
    36987-2376Giant Wild RyeGiant Wild Rye
    36987-2377Giant Wild RyeGiant Wild Rye
    36987-2378Giant Wild RyeGiant Wild Rye
    36987-2379Giant Wild RyeGiant Wild Rye
    36987-2380Giant Wild RyeGiant Wild Rye

    © 2024 FDA.report
    This site is not affiliated with or endorsed by the FDA.