22840-9669 : Rhizopus Mix Intradermal; Percutaneous; Subcutaneous Solution


NDC: 22840-9669
Labeler: Greer Laboratories, Inc.
Product Type: Non-standardized Allergenic
Drug Name: Rhizopus Mix
Dosage Form: Intradermal; Percutaneous; Subcutaneous Solution
Application #: BLA101833
Rev. Date: 


NDC Package Codes:

  • 22840-9669-2: 10 ML IN 1 VIAL, MULTI‑DOSE (22840‑9669‑2)
  • 22840-9669-4: 50 ML IN 1 VIAL, MULTI‑DOSE (22840‑9669‑4)
  • 22840-9669-5: 5 ML IN 1 BOTTLE, DROPPER (22840‑9669‑5)

Active Ingredients:

  • Rhizopus Arrhizus
  • Rhizopus Stolonifer

Dosage Strength:

  • .0125 g/mL
  • .0125 g/mL

Pharmaceutical Classes:

  • Allergens [CS]
  • Allergens [Chemical/Ingredient]
  • Cell-mediated Immunity [PE]
  • Fungal Proteins [CS]
  • Fungal Proteins [Chemical/Ingredient]
  • Increased Histamine Release [PE]
  • Increased IgG Production [PE]
  • Non-Standardized Fungal Allergenic Extract [EPC]

Related Products:

Based on records with the same trade name.
  • 22840-9665 Rhizopus Mix Intradermal; Percutaneous; Subcutaneous Solution by Greer Laboratories, Inc.
  • 22840-9666 Rhizopus Mix Intradermal; Percutaneous; Subcutaneous Solution by Greer Laboratories, Inc.
  • 22840-9668 Rhizopus Mix Intradermal; Percutaneous; Subcutaneous Solution by Greer Laboratories, Inc.
  • 22840-9680 Rhizopus Mix Intradermal; Percutaneous; Subcutaneous Solution by Greer Laboratories, Inc.

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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.