22840-5780 : Tuna .05 g/ml Intradermal; Percutaneous; Subcutaneous Solution


NDC: 22840-5780
Labeler: Greer Laboratories, Inc.
Product Type: Non-standardized Allergenic
Drug Name: Tuna
Dosage Form: Intradermal; Percutaneous; Subcutaneous Solution
Application #: BLA101833
Rev. Date: 


NDC Package Codes:

  • 22840-5780-2: 10 ML IN 1 VIAL, MULTI‑DOSE (22840‑5780‑2)
  • 22840-5780-5: 5 ML IN 1 BOTTLE, DROPPER (22840‑5780‑5)

Active Ingredients:

  • Yellowfin Tuna

Dosage Strength:

  • .05 g/mL

Pharmaceutical Classes:

  • Allergens [CS]
  • Cell-mediated Immunity [PE]
  • Dietary Proteins [CS]
  • Fish Proteins
  • Dietary [EXT]
  • Increased Histamine Release [PE]
  • Non-Standardized Food Allergenic Extract [EPC]

Related Products:

Based on records with the same trade name.
  • 0268-6226 Tuna .1 g/ml Percutaneous Injection, Solution by Alk-abello, Inc.
  • 49288-0569 Tuna .05 g/ml Intradermal; Subcutaneous Injection, Solution by Antigen Laboratories, Inc.
  • 54575-468 Tuna 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.