NDC 49288-0341

Standardized Orchard Grass Pollen

Standardized Orchard Grass Pollen

Standardized Orchard Grass Pollen is a Intradermal; Subcutaneous Injection, Solution in the Human Prescription Drug category. It is labeled and distributed by Antigen Laboratories, Inc.. The primary component is Dactylis Glomerata Pollen.

Product ID49288-0341_bb0c98b2-aaa8-49c4-887a-928e3937769c
NDC49288-0341
Product TypeHuman Prescription Drug
Proprietary NameStandardized Orchard Grass Pollen
Generic NameStandardized Orchard Grass Pollen
Dosage FormInjection, Solution
Route of AdministrationINTRADERMAL; SUBCUTANEOUS
Marketing Start Date1997-06-13
Marketing CategoryBLA / BLA
Application NumberBLA102228
Labeler NameAntigen Laboratories, Inc.
Substance NameDACTYLIS GLOMERATA POLLEN
Active Ingredient Strength100000 [BAU]/mL
Pharm ClassesStandardized 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 49288-0341-2

5 mL in 1 VIAL, MULTI-DOSE (49288-0341-2)
Marketing Start Date1997-06-13
NDC Exclude FlagN
Sample Package?N

NDC SPL Data Element Entries

NDC 49288-0341-5 [49288034105]

Standardized Orchard Grass Pollen INJECTION, SOLUTION
Marketing CategoryBLA
Application NumberBLA102228
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date1997-06-13
Inactivation Date2019-10-21

NDC 49288-0341-3 [49288034103]

Standardized Orchard Grass Pollen INJECTION, SOLUTION
Marketing CategoryBLA
Application NumberBLA102228
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date1997-06-13
Inactivation Date2019-10-21

NDC 49288-0341-4 [49288034104]

Standardized Orchard Grass Pollen INJECTION, SOLUTION
Marketing CategoryBLA
Application NumberBLA102228
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date1997-06-13
Inactivation Date2019-10-21

NDC 49288-0341-2 [49288034102]

Standardized Orchard Grass Pollen INJECTION, SOLUTION
Marketing CategoryBLA
Application NumberBLA102228
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date1997-06-13
Inactivation Date2019-10-21

Drug Details

Active Ingredients

IngredientStrength
DACTYLIS GLOMERATA POLLEN100000 [BAU]/mL

OpenFDA Data

SPL SET ID:c08f73ff-4f15-449c-9507-c422367f106b
Manufacturer
UNII
RxNorm Concept Unique ID - RxCUI
  • 853027
  • 854054
  • 851873
  • 853047
  • 897496
  • 854162
  • 853278
  • 852157
  • Pharmacological Class

    • 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 "Standardized Orchard Grass Pollen" or generic name "Standardized Orchard Grass Pollen"

    NDCBrand NameGeneric Name
    22840-0205Standardized Orchard Grass PollenDactylis glomerata
    22840-0206Standardized Orchard Grass PollenDactylis glomerata
    36987-2345Standardized Orchard Grass PollenStandardized Orchard Grass Pollen
    36987-2346Standardized Orchard Grass PollenStandardized Orchard Grass Pollen
    49288-0341Standardized Orchard Grass PollenStandardized Orchard Grass Pollen
    54575-097STANDARDIZED ORCHARD GRASS POLLENDactylis glomerata pollen

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