49288-0569 : Tuna .05 g/ml Intradermal; Subcutaneous Injection, Solution


NDC: 49288-0569
Labeler: Antigen Laboratories, Inc.
Product Type: Non-standardized Allergenic
Drug Name: Tuna
Dosage Form: Intradermal; Subcutaneous Injection, Solution
Application #: BLA102223
Rev. Date: 


NDC Package Codes:

  • 49288-0569-1: 2 ML IN 1 VIAL, MULTI‑DOSE (49288‑0569‑1)
  • 49288-0569-2: 5 ML IN 1 VIAL, MULTI‑DOSE (49288‑0569‑2)
  • 49288-0569-3: 10 ML IN 1 VIAL, MULTI‑DOSE (49288‑0569‑3)
  • 49288-0569-4: 30 ML IN 1 VIAL, MULTI‑DOSE (49288‑0569‑4)
  • 49288-0569-5: 50 ML IN 1 VIAL, MULTI‑DOSE (49288‑0569‑5)

Active Ingredients:

  • Tuna

Dosage Strength:

  • .05 g/mL

Pharmaceutical Classes:

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

Related Products:

Based on records with the same trade name.
  • 0268-6226 Tuna .1 g/ml Percutaneous Injection, Solution by Alk-abello, Inc.
  • 22840-5780 Tuna .05 g/ml Intradermal; Percutaneous; Subcutaneous Solution by Greer 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.