22840-2666 : Epidermophyton Floccosum .1 g/ml Intradermal; Percutaneous; Subcutaneous Solution


NDC: 22840-2666
Labeler: Greer Laboratories, Inc.
Product Type: Non-standardized Allergenic
Drug Name: Epidermophyton Floccosum
Dosage Form: Intradermal; Percutaneous; Subcutaneous Solution
Application #: BLA101833
Rev. Date: 


NDC Package Codes:

  • 22840-2666-2: 10 ML IN 1 VIAL, MULTI‑DOSE (22840‑2666‑2)

Active Ingredients:

  • Epidermophyton Floccosum

Dosage Strength:

  • .1 g/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.
  • 22840-1667 Epidermophyton Floccosum .05 g/ml Intradermal; Percutaneous; Subcutaneous Solution by Greer Laboratories, Inc.
  • 22840-1668 Epidermophyton Floccosum .001 g/ml Intradermal; Percutaneous; Subcutaneous Solution by Greer Laboratories, Inc.
  • 22840-1669 Epidermophyton Floccosum 1000 [Pnu]/Ml Intradermal; Percutaneous; Subcutaneous Solution by Greer Laboratories, Inc.
  • 22840-5617 Epidermophyton Floccosum .05 g/ml Intradermal; Percutaneous; Subcutaneous Solution by Greer Laboratories, Inc.
  • 54575-195 Epidermophyton Floccosum 1 g/20ml Percutaneous; Subcutaneous Injection, Solution by Allergy 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.