NDC 36987-3278

California Mugwort

California Mugwort

California 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 Douglasiana Pollen.

Product ID36987-3278_afd9ee5b-b6ea-4bde-af79-31cf9b90dabb
NDC36987-3278
Product TypeHuman Prescription Drug
Proprietary NameCalifornia Mugwort
Generic NameCalifornia Mugwort
Dosage FormInjection, Solution
Route of AdministrationINTRADERMAL; SUBCUTANEOUS
Marketing Start Date1972-08-29
Marketing CategoryBLA / BLA
Application NumberBLA102192
Labeler NameNelco Laboratories, Inc.
Substance NameARTEMISIA DOUGLASIANA POLLEN
Active Ingredient Strength10000 [PNU]/mL
Pharm ClassesNon-Standardized Pollen Allergenic Extract [EPC],Increased Histamine Release [PE],Increased IgG Production [PE],Pollen [CS],Allergens [CS],Cell-mediated Immunity [PE]
NDC Exclude FlagE
Listing Certified Through2017-12-31

Packaging

NDC 36987-3278-3

30 mL in 1 VIAL, MULTI-DOSE (36987-3278-3)
Marketing Start Date1972-08-29
NDC Exclude FlagN
Sample Package?N

NDC SPL Data Element Entries

NDC 36987-3278-4 [36987327804]

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

NDC 36987-3278-3 [36987327803]

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

NDC 36987-3278-1 [36987327801]

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

NDC 36987-3278-2 [36987327802]

California 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 DOUGLASIANA POLLEN10000 [PNU]/mL

OpenFDA Data

SPL SET ID:e1a0f4d9-3bd9-4cf9-a09e-359015738c38
Manufacturer
UNII
RxNorm Concept Unique ID - RxCUI
  • 894818
  • Pharmacological Class

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

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

    NDCBrand NameGeneric Name
    36987-3277California MugwortCalifornia Mugwort
    36987-3278California MugwortCalifornia Mugwort
    36987-3279California MugwortCalifornia Mugwort
    36987-3280California MugwortCalifornia Mugwort
    36987-3281California MugwortCalifornia Mugwort
    36987-3282California MugwortCalifornia Mugwort
    36987-3283California MugwortCalifornia Mugwort
    36987-3284California MugwortCalifornia Mugwort

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