NDC 36987-3290

Darkleaves Mugwort

Darkleaves Mugwort

Darkleaves Mugwort 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 Artemisia Ludoviciana Pollen.

Product ID36987-3290_c6c9737f-cac3-445a-b895-e2dacca18a0f
NDC36987-3290
Product TypeHuman Prescription Drug
Proprietary NameDarkleaves Mugwort
Generic NameDarkleaves Mugwort
Dosage FormInjection, Solution
Route of AdministrationINTRADERMAL; SUBCUTANEOUS
Marketing Start Date1972-08-29
Marketing CategoryBLA / BLA
Application NumberBLA102192
Labeler NameNelco Laboratories, Inc.
Substance NameARTEMISIA LUDOVICIANA POLLEN
Active Ingredient Strength0 g/mL
Pharm ClassesNon-Standardized Pollen Allergenic Extract [EPC],Increased Histamine Release [PE],Cell-mediated Immunity [PE],Pollen [CS],Allergens [CS]
NDC Exclude FlagE
Listing Certified Through2017-12-31

Packaging

NDC 36987-3290-1

5 mL in 1 VIAL, MULTI-DOSE (36987-3290-1)
Marketing Start Date1972-08-29
NDC Exclude FlagN
Sample Package?N

NDC SPL Data Element Entries

NDC 36987-3290-2 [36987329002]

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

NDC 36987-3290-1 [36987329001]

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

NDC 36987-3290-3 [36987329003]

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

NDC 36987-3290-4 [36987329004]

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

Drug Details

Active Ingredients

IngredientStrength
ARTEMISIA LUDOVICIANA POLLEN.05 g/mL

OpenFDA Data

SPL SET ID:ccd1d7d8-c5de-4cdb-b1e7-a3b114394fd4
Manufacturer
UNII
RxNorm Concept Unique ID - RxCUI
  • 851933
  • 852049
  • 851937
  • 852327
  • 852596
  • 897335
  • 852535
  • 995746
  • 852082
  • 897394
  • 852240
  • 897506
  • 897319
  • 851929
  • 852010
  • 851988
  • 896249
  • 852155
  • 851893
  • 852216
  • 851897
  • 852212
  • 852745
  • 851941
  • 852529
  • 852077
  • 852099
  • 897307
  • 852542
  • 852554
  • 895922
  • 852001
  • 852161
  • 852032
  • 851972
  • 852023
  • 995604
  • Pharmacological Class

    • Non-Standardized Pollen Allergenic Extract [EPC]
    • Increased Histamine Release [PE]
    • Cell-mediated Immunity [PE]
    • Pollen [CS]
    • Allergens [CS]

    NDC Crossover Matching brand name "Darkleaves Mugwort" or generic name "Darkleaves Mugwort"

    NDCBrand NameGeneric Name
    36987-3285Darkleaves MugwortDarkleaves Mugwort
    36987-3286Darkleaves MugwortDarkleaves Mugwort
    36987-3287Darkleaves MugwortDarkleaves Mugwort
    36987-3288Darkleaves MugwortDarkleaves Mugwort
    36987-3289Darkleaves MugwortDarkleaves Mugwort
    36987-3290Darkleaves MugwortDarkleaves Mugwort
    36987-3291Darkleaves MugwortDarkleaves Mugwort
    36987-3292Darkleaves MugwortDarkleaves Mugwort

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