NDC 36987-3201

Firebush/Burning Bush

Firebush/burning Bush

Firebush/Burning Bush 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 Kochia Scoparia Pollen.

Product ID36987-3201_39113b10-fd1f-4cfc-8432-755a1686fcc4
NDC36987-3201
Product TypeHuman Prescription Drug
Proprietary NameFirebush/Burning Bush
Generic NameFirebush/burning Bush
Dosage FormInjection, Solution
Route of AdministrationINTRADERMAL; SUBCUTANEOUS
Marketing Start Date1972-08-29
Marketing CategoryBLA / BLA
Application NumberBLA102192
Labeler NameNelco Laboratories, Inc.
Substance NameKOCHIA SCOPARIA 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 36987-3201-2

10 mL in 1 VIAL, MULTI-DOSE (36987-3201-2)
Marketing Start Date1972-08-29
NDC Exclude FlagN
Sample Package?N

NDC SPL Data Element Entries

NDC 36987-3201-1 [36987320101]

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

NDC 36987-3201-3 [36987320103]

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

NDC 36987-3201-4 [36987320104]

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

NDC 36987-3201-2 [36987320102]

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

Drug Details

Active Ingredients

IngredientStrength
KOCHIA SCOPARIA 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 "Firebush/Burning Bush" or generic name "Firebush/burning Bush"

    NDCBrand NameGeneric Name
    36987-3197Firebush/Burning BushFirebush/Burning Bush
    36987-3198Firebush/Burning BushFirebush/Burning Bush
    36987-3199Firebush/Burning BushFirebush/Burning Bush
    36987-3200Firebush/Burning BushFirebush/Burning Bush
    36987-3201Firebush/Burning BushFirebush/Burning Bush
    36987-3202Firebush/Burning BushFirebush/Burning Bush
    36987-3203Firebush/Burning BushFirebush/Burning Bush
    36987-3204Firebush/Burning BushFirebush/Burning Bush

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