22840-5642 : Mycogone Perniciosa .05 g/ml Intradermal; Percutaneous; Subcutaneous Solution


NDC: 22840-5642
Labeler: Greer Laboratories, Inc.
Product Type: Non-standardized Allergenic
Drug Name: Mycogone Perniciosa
Dosage Form: Intradermal; Percutaneous; Subcutaneous Solution
Application #: BLA101833
Rev. Date: 


NDC Package Codes:

  • 22840-5642-2: 10 ML IN 1 VIAL, MULTI‑DOSE (22840‑5642‑2)
  • 22840-5642-4: 50 ML IN 1 VIAL, MULTI‑DOSE (22840‑5642‑4)
  • 22840-5642-5: 5 ML IN 1 BOTTLE, DROPPER (22840‑5642‑5)

Active Ingredients:

  • Hypomyces Perniciosus

Dosage Strength:

  • .05 g/mL

Pharmaceutical Classes:

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

Related Products:

Based on records with the same trade name.
  • 49288-0296 Mycogone Perniciosa .1 g/ml Intradermal; Subcutaneous Injection, Solution by Antigen Laboratories, Inc.
  • 49288-0297 Mycogone Perniciosa .05 g/ml Intradermal; Subcutaneous Injection, Solution by Antigen 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.