49288-0685 : Treatment Set Ts333001 Intradermal; Subcutaneous Injection, Solution


NDC: 49288-0685
Labeler: Antigen Laboratories, Inc.
Product Type: Human Prescription Drug
Drug Name: Treatment Set Ts333001
Dosage Form: Intradermal; Subcutaneous Injection, Solution
Application #: BLA102223
Rev. Date: 


NDC Package Codes:

  • 49288-0685-3: 10 ML IN 1 VIAL, MULTI‑DOSE (49288‑0685‑3)

Active Ingredients:

  • Amaranthus Retroflexus Pollen
  • Ambrosia Artemisiifolia Pollen
  • Canis Lupus Familiaris Hair
  • Carya Alba Pollen
  • Celtis Occidentalis Pollen
  • Felis Catus Hair
  • Juglans Californica Pollen
  • Phleum Pratense Pollen
  • Plantago Lanceolata Pollen
  • Platanus Occidentalis Pollen
  • Quercus Alba Pollen
  • Rumex Acetosella Pollen
  • Salsola Kali Pollen
  • Urtica Dioica Pollen

Dosage Strength:

  • .002 g/mL
  • 4000 [AU]/mL
  • .002 g/mL
  • .002 g/mL
  • .002 g/mL
  • 400 [BAU]/mL
  • .002 g/mL
  • 4000 [BAU]/mL
  • .002 g/mL
  • .002 g/mL
  • .002 g/mL
  • .002 g/mL
  • .002 g/mL
  • .002 g/mL

Pharmaceutical Classes:

  • Standardized Animal Hair Allergenic Extract [EPC]
  • Increased Histamine Release [PE]
  • Cell-mediated Immunity [PE]
  • Increased IgG Production [PE]
  • Dander [CS]
  • Allergens [CS]
  • Salivary Proteins and Peptides [CS]
  • Non-Standardized Animal Hair Allergenic Extract [EPC]
  • Animal Fur [CS]
  • Standardized Pollen Allergenic Extract [EPC]
  • Pollen [CS]
  • Non-Standardized Pollen Allergenic Extract [EPC]

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.