NDC 36987-3361

Ailanthus

Ailanthus

Ailanthus 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 Ailanthus Altissima Pollen.

Product ID36987-3361_39113b10-fd1f-4cfc-8432-755a1686fcc4
NDC36987-3361
Product TypeHuman Prescription Drug
Proprietary NameAilanthus
Generic NameAilanthus
Dosage FormInjection, Solution
Route of AdministrationINTRADERMAL; SUBCUTANEOUS
Marketing Start Date1972-08-29
Marketing CategoryBLA / BLA
Application NumberBLA102192
Labeler NameNelco Laboratories, Inc.
Substance NameAILANTHUS ALTISSIMA POLLEN
Active Ingredient Strength40000 [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 36987-3361-2

10 mL in 1 VIAL, MULTI-DOSE (36987-3361-2)
Marketing Start Date1972-08-29
NDC Exclude FlagN
Sample Package?N

NDC SPL Data Element Entries

NDC 36987-3361-4 [36987336104]

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

NDC 36987-3361-1 [36987336101]

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

NDC 36987-3361-3 [36987336103]

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

NDC 36987-3361-2 [36987336102]

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

Drug Details

Active Ingredients

IngredientStrength
AILANTHUS ALTISSIMA POLLEN40000 [PNU]/mL

OpenFDA Data

SPL SET ID:a63e5aef-44c2-4f90-a33d-91ec10298089
Manufacturer
UNII
RxNorm Concept Unique ID - RxCUI
  • 897968
  • 896133
  • 897315
  • 896281
  • 1006367
  • 895914
  • 895614
  • 896290
  • 1006488
  • 895679
  • 896265
  • 897977
  • 896302
  • 896080
  • 897402
  • 1013974
  • 897959
  • 897951
  • 896198
  • 897998
  • 901477
  • 896173
  • 896158
  • 1006359
  • 897376
  • 897327
  • 1013976
  • 896211
  • 895728
  • 897343
  • 897533
  • 898339
  • 896114
  • 896257
  • 901495
  • 897384
  • 1013991
  • 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 "Ailanthus" or generic name "Ailanthus"

    NDCBrand NameGeneric Name
    36987-3357AilanthusAilanthus
    36987-3358AilanthusAilanthus
    36987-3359AilanthusAilanthus
    36987-3360AilanthusAilanthus
    36987-3361AilanthusAilanthus
    36987-3362AilanthusAilanthus
    36987-3363AilanthusAilanthus
    36987-3364AilanthusAilanthus
    68428-186AilanthusAILANTHUS ALTISSIMA FLOWERING TWIG

    Trademark Results [Ailanthus]

    Mark Image

    Registration | Serial
    Company
    Trademark
    Application Date
    AILANTHUS
    AILANTHUS
    98712641 not registered Live/Pending
    Ailanthus BK LLC
    2024-08-22

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