49288-0949 : Treatment Set Ts351031 Intradermal; Subcutaneous Injection, Solution


NDC49288-0949
Labeler: Antigen Laboratories, Inc.
Product Type: Non-standardized Allergenic
Drug Name: Treatment Set Ts351031
Dosage Form: Intradermal; Subcutaneous Injection, Solution
Application #: BLA102223
Rev. Date: 


NDC Package Codes:

  • 49288-0949-3: 10 ML IN 1 VIAL, MULTI‑DOSE (49288‑0949‑3)

Active Ingredients:

  • Acer Negundo Pollen
  • Amaranthus Retroflexus Pollen
  • Ambrosia Artemisiifolia Pollen
  • Ambrosia Psilostachya Pollen
  • Ambrosia Trifida Pollen
  • Betula Nigra Pollen
  • Carya Alba Pollen
  • Carya Illinoinensis Pollen
  • Chenopodium Album Pollen
  • Fraxinus Americana Pollen
  • Iva Annua Var. Annua Pollen
  • Juniperus Virginiana Pollen
  • Kochia Scoparia Pollen
  • Plantago Lanceolata Pollen
  • Poa Pratensis Pollen
  • Populus Deltoides Pollen
  • Quercus Alba Pollen
  • Rumex Acetosella Pollen
  • Salsola Kali Pollen
  • Sorghum Halepense Pollen
  • Ulmus Americana Pollen

Dosage Strength:

  • .0004 g/mL
  • .002 g/mL
  • .000027 g/mL
  • .000027 g/mL
  • .000027 g/mL
  • .00008 g/mL
  • .0002 g/mL
  • .0002 g/mL
  • .002 g/mL
  • .00008 g/mL
  • .002 g/mL
  • .00008 g/mL
  • .002 g/mL
  • .00008 g/mL
  • 160 [BAU]/mL
  • .00008 g/mL
  • .00008 g/mL
  • .0004 g/mL
  • .002 g/mL
  • .0004 g/mL
  • .002 g/mL

Pharmaceutical Classes:

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

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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.