49288-0236 : Mixture of Eight Standardized Grasses Intradermal; Subcutaneous Injection, Solution


NDC: 49288-0236
Labeler: Antigen Laboratories, Inc.
Product Type: Human Prescription Drug
Drug Name: Mixture of Eight Standardized Grasses
Dosage Form: Intradermal; Subcutaneous Injection, Solution
Application #: BLA102226
Rev. Date: 


NDC Package Codes:

  • 49288-0236-3: 10 ML IN 1 VIAL, MULTI‑DOSE (49288‑0236‑3)
  • 49288-0236-4: 30 ML IN 1 VIAL, MULTI‑DOSE (49288‑0236‑4)
  • 49288-0236-5: 50 ML IN 1 VIAL, MULTI‑DOSE (49288‑0236‑5)

Active Ingredients:

  • Agrostis Gigantea Pollen
  • Anthoxanthum Odoratum Pollen
  • Cynodon Dactylon Pollen
  • Dactylis Glomerata Pollen
  • Festuca Pratensis Pollen
  • Lolium Perenne Pollen
  • Phleum Pratense Pollen
  • Poa Pratensis Pollen

Dosage Strength:

  • 12500 [BAU]/mL
  • 12500 [BAU]/mL
  • 1250 [BAU]/mL
  • 12500 [BAU]/mL
  • 12500 [BAU]/mL
  • 12500 [BAU]/mL
  • 12500 [BAU]/mL
  • 12500 [BAU]/mL

Pharmaceutical Classes:

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