NDC 36987-2287

Brome Grass

Brome Grass

Brome Grass 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 Bromus Inermis Pollen.

Product ID36987-2287_43e1cd4a-c8eb-4acd-bee8-f61ab9b5cdac
NDC36987-2287
Product TypeHuman Prescription Drug
Proprietary NameBrome Grass
Generic NameBrome Grass
Dosage FormInjection, Solution
Route of AdministrationINTRADERMAL; SUBCUTANEOUS
Marketing Start Date1972-08-29
Marketing CategoryBLA / BLA
Application NumberBLA102192
Labeler NameNelco Laboratories, Inc.
Substance NameBROMUS INERMIS POLLEN
Active Ingredient Strength10000 [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],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 36987-2287-2

10 mL in 1 VIAL, MULTI-DOSE (36987-2287-2)
Marketing Start Date1972-08-29
NDC Exclude FlagN
Sample Package?N

NDC SPL Data Element Entries

NDC 36987-2287-3 [36987228703]

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

NDC 36987-2287-2 [36987228702]

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

NDC 36987-2287-1 [36987228701]

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

NDC 36987-2287-4 [36987228704]

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

Drug Details

Active Ingredients

IngredientStrength
BROMUS INERMIS POLLEN10000 [PNU]/mL

OpenFDA Data

SPL SET ID:0e31061a-dd28-4932-ae30-f95c3c1f1b11
Manufacturer
UNII
RxNorm Concept Unique ID - RxCUI
  • 1044502
  • 897349
  • 889567
  • 1044523
  • 897357
  • 889668
  • 900010
  • 1014345
  • 899974
  • 1044252
  • 1000015
  • 900155
  • 898134
  • 897331
  • 1044494
  • 889532
  • 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 "Brome Grass" or generic name "Brome Grass"

    NDCBrand NameGeneric Name
    36987-2287Brome GrassBrome Grass
    36987-2288Brome GrassBrome Grass
    36987-2289Brome GrassBrome Grass
    36987-2290Brome GrassBrome Grass
    36987-2291Brome GrassBrome Grass
    36987-2292Brome GrassBrome Grass
    36987-2293Brome GrassBrome Grass
    36987-2294Brome GrassBrome Grass
    0268-1086BROMUS INERMIS POLLENBrome Grass
    0268-1087BROMUS INERMIS POLLENBrome Grass
    0268-1089BROMUS INERMIS POLLENBrome Grass
    0268-6691BROMUS INERMIS POLLENBrome Grass
    0268-6692BROMUS INERMIS POLLENBrome Grass

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