NDC 36987-2286

Canadian Blue Grass

Canadian Blue Grass

Canadian Blue 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 Poa Compressa Pollen.

Product ID36987-2286_b28ad23e-222c-49fb-8631-a50fe06898eb
NDC36987-2286
Product TypeHuman Prescription Drug
Proprietary NameCanadian Blue Grass
Generic NameCanadian Blue Grass
Dosage FormInjection, Solution
Route of AdministrationINTRADERMAL; SUBCUTANEOUS
Marketing Start Date1972-08-29
Marketing CategoryBLA / BLA
Application NumberBLA102192
Labeler NameNelco Laboratories, Inc.
Substance NamePOA COMPRESSA 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 36987-2286-1

5 mL in 1 VIAL, MULTI-DOSE (36987-2286-1)
Marketing Start Date1972-08-29
NDC Exclude FlagN
Sample Package?N

NDC SPL Data Element Entries

NDC 36987-2286-3 [36987228603]

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

NDC 36987-2286-1 [36987228601]

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

NDC 36987-2286-4 [36987228604]

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

NDC 36987-2286-2 [36987228602]

Canadian Blue 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
POA COMPRESSA POLLEN.1 g/mL

OpenFDA Data

SPL SET ID:701a1bc2-06dd-40e3-a7ff-1ac9d349242e
Manufacturer
UNII
RxNorm Concept Unique ID - RxCUI
  • 889571
  • 1044500
  • 1044521
  • 900008
  • 889671
  • 897347
  • 897355
  • 899972
  • 1014695
  • 897329
  • 1044240
  • 889534
  • 1044250
  • 900153
  • 898132
  • 1044492
  • 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 "Canadian Blue Grass" or generic name "Canadian Blue Grass"

    NDCBrand NameGeneric Name
    36987-2279Canadian Blue GrassCanadian Blue Grass
    36987-2280Canadian Blue GrassCanadian Blue Grass
    36987-2281Canadian Blue GrassCanadian Blue Grass
    36987-2282Canadian Blue GrassCanadian Blue Grass
    36987-2283Canadian Blue GrassCanadian Blue Grass
    36987-2284Canadian Blue GrassCanadian Blue Grass
    36987-2285Canadian Blue GrassCanadian Blue Grass
    36987-2286Canadian Blue GrassCanadian Blue Grass

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