49288-0959 : Treatment Set Ts351314 Intradermal; Subcutaneous Injection, Solution


NDC: 49288-0959
Labeler: Antigen Laboratories, Inc.
Product Type: Non-standardized Allergenic
Drug Name: Treatment Set Ts351314
Dosage Form: Intradermal; Subcutaneous Injection, Solution
Application #: BLA102223
Rev. Date: 


NDC Package Codes:

  • 49288-0959-3: 10 ML IN 1 VIAL, MULTI‑DOSE (49288‑0959‑3)

Active Ingredients:

  • Acer Negundo Pollen
  • Amaranthus Retroflexus Pollen
  • Ambrosia Artemisiifolia Pollen
  • Betula Populifolia Pollen
  • Carya Alba Pollen
  • Carya Illinoinensis Pollen
  • Chenopodium Album Pollen
  • Fraxinus Americana Pollen
  • Juglans Nigra Pollen
  • Juniperus Virginiana Pollen
  • Morus Rubra Pollen
  • Plantago Lanceolata Pollen
  • Platanus Occidentalis Pollen
  • Populus Deltoides Pollen
  • Quercus Alba Pollen
  • Rumex Acetosella Pollen
  • Ulmus Americana Pollen
  • Urtica Dioica Pollen

Dosage Strength:

  • .0004 g/mL
  • .00008 g/mL
  • 4000 [AU]/mL
  • .00008 g/mL
  • .00004 g/mL
  • .00004 g/mL
  • .002 g/mL
  • .0004 g/mL
  • .002 g/mL
  • .002 g/mL
  • .0004 g/mL
  • .002 g/mL
  • .002 g/mL
  • .0004 g/mL
  • .00008 g/mL
  • .000008 g/mL
  • .0004 g/mL
  • .002 g/mL

Pharmaceutical Classes:

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

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Note: The RxChat NDC Database uses publicly available data from the FDA and the U.S. National Library of Medicine (NLM); The NLM is not responsible for the data presented and does not endorse or recommend this or any other product. While we make every effort to ensure that the information presented is accurate, you should assume that all results are unvalidated. To report any errors or inconsistencies please contact us.