NDC 36987-2292

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 ID36987-2292_72e454d7-3ef9-4e04-bd95-d894fab0b155
NDC36987-2292
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 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 36987-2292-2

10 mL in 1 VIAL, MULTI-DOSE (36987-2292-2)
Marketing Start Date1972-08-29
NDC Exclude FlagN
Sample Package?N

NDC SPL Data Element Entries

NDC 36987-2292-3 [36987229203]

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

NDC 36987-2292-2 [36987229202]

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

NDC 36987-2292-1 [36987229201]

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

NDC 36987-2292-4 [36987229204]

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 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 "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

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