22840-9643 : Monilia Mix Intradermal; Percutaneous; Subcutaneous Solution


NDC: 22840-9643
Labeler: Greer Laboratories, Inc.
Product Type: Non-standardized Allergenic
Drug Name: Monilia Mix
Dosage Form: Intradermal; Percutaneous; Subcutaneous Solution
Application #: BLA101833
Rev. Date: 


NDC Package Codes:

  • 22840-9643-1: 5 ML IN 1 VIAL, MULTI‑DOSE (22840‑9643‑1)

Active Ingredients:

  • Candida Albicans
  • Neurospora Intermedia

Dosage Strength:

  • 500 [PNU]/mL
  • 500 [PNU]/mL

Pharmaceutical Classes:

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

Related Products:

Based on records with the same trade name.
  • 22840-9642 Monilia Mix Intradermal; Percutaneous; Subcutaneous Solution by Greer Laboratories, Inc.
  • 22840-9644 Monilia Mix Intradermal; Percutaneous; Subcutaneous Solution by Greer Laboratories, Inc.
  • 22840-9645 Monilia Mix Intradermal; Percutaneous; Subcutaneous Solution by Greer Laboratories, Inc.
  • 22840-9677 Monilia 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.