NDC 49288-0403

Pyrethrum

Pyrethrum

Pyrethrum 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 Pyrethrum Cinerariifolium.

Product ID49288-0403_3af4be6b-c022-4834-9006-f6cc8d8041da
NDC49288-0403
Product TypeHuman Prescription Drug
Proprietary NamePyrethrum
Generic NamePyrethrum
Dosage FormInjection, Solution
Route of AdministrationINTRADERMAL; SUBCUTANEOUS
Marketing Start Date1974-03-23
Marketing CategoryBLA / BLA
Application NumberBLA102223
Labeler NameAntigen Laboratories, Inc.
Substance NamePYRETHRUM CINERARIIFOLIUM
Active Ingredient Strength0 g/mL
Pharm ClassesNon-Standardized Plant Allergenic Extract [EPC],Increased Histamine Release [PE],Cell-mediated Immunity [PE],Increased IgG Production [PE],Allergens [CS],Plant Proteins [CS]
NDC Exclude FlagE
Listing Certified Through2017-12-31

Packaging

NDC 49288-0403-4

30 mL in 1 VIAL, MULTI-DOSE (49288-0403-4)
Marketing Start Date1974-03-23
NDC Exclude FlagN
Sample Package?N

NDC SPL Data Element Entries

NDC 49288-0403-1 [49288040301]

Pyrethrum INJECTION, SOLUTION
Marketing CategoryBLA
Application NumberBLA102223
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date1974-03-23
Inactivation Date2019-10-21

NDC 49288-0403-5 [49288040305]

Pyrethrum INJECTION, SOLUTION
Marketing CategoryBLA
Application NumberBLA102223
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date1974-03-23
Inactivation Date2019-10-21

NDC 49288-0403-3 [49288040303]

Pyrethrum INJECTION, SOLUTION
Marketing CategoryBLA
Application NumberBLA102223
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date1974-03-23
Inactivation Date2019-10-21

NDC 49288-0403-2 [49288040302]

Pyrethrum INJECTION, SOLUTION
Marketing CategoryBLA
Application NumberBLA102223
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date1974-03-23
Inactivation Date2019-10-21

NDC 49288-0403-4 [49288040304]

Pyrethrum INJECTION, SOLUTION
Marketing CategoryBLA
Application NumberBLA102223
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date1974-03-23
Inactivation Date2019-10-21

Drug Details

Active Ingredients

IngredientStrength
PYRETHRUM CINERARIIFOLIUM.05 g/mL

OpenFDA Data

SPL SET ID:d71013ab-718c-4cb0-ae1a-31fdd6db8851
Manufacturer
UNII
RxNorm Concept Unique ID - RxCUI
  • 967973
  • 889598
  • 966928
  • 968497
  • 1098356
  • 904965
  • 852065
  • 1014199
  • 852547
  • Pharmacological Class

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

    NDC Crossover Matching brand name "Pyrethrum" or generic name "Pyrethrum"

    NDCBrand NameGeneric Name
    22840-1533PyrethrumChrysanthemum cinerariifolium
    22840-1535PyrethrumChrysanthemum cinerariifolium
    22840-1559PyrethrumChrysanthemum cinerariifolium
    22840-5516PyrethrumChrysanthemum cinerariifolium
    49288-0403PyrethrumPyrethrum
    54575-273PYRETHRUMtanacetum cinerariifolium flower
    0268-6318PYRETHRUM CINERARIIFOLIUMPyrethrum

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