49288-0759 : Treatment Set Ts333374 Intradermal; Subcutaneous Injection, Solution


NDC: 49288-0759
Labeler: Antigen Laboratories, Inc.
Product Type: Human Prescription Drug
Drug Name: Treatment Set Ts333374
Dosage Form: Intradermal; Subcutaneous Injection, Solution
Application #: BLA102223
Rev. Date: 


NDC Package Codes:

  • 49288-0759-3: 10 ML IN 1 VIAL, MULTI‑DOSE (49288‑0759‑3)

Active Ingredients:

  • Acer Negundo Pollen
  • Ambrosia Artemisiifolia Pollen
  • Ambrosia Psilostachya Pollen
  • Ambrosia Trifida Pollen
  • Betula Nigra Pollen
  • Chenopodium Album Pollen
  • Cynodon Dactylon Pollen
  • Fraxinus Americana Pollen
  • Iva Annua Var. Annua Pollen
  • Juniperus Virginiana Pollen
  • Plantago Lanceolata Pollen
  • Poa Pratensis Pollen
  • Sorghum Halepense Pollen

Dosage Strength:

  • .00008 g/mL
  • .00067 g/mL
  • .00067 g/mL
  • .00067 g/mL
  • .002 g/mL
  • .002 g/mL
  • 16 [BAU]/mL
  • .00008 g/mL
  • .002 g/mL
  • .00008 g/mL
  • .00008 g/mL
  • 4000 [BAU]/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]

NDC QR Code

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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.