49288-0044 : Mung Bean .05 g/ml Intradermal; Subcutaneous Injection, Solution


NDC: 49288-0044
Labeler: Antigen Laboratories, Inc.
Product Type: Human Prescription Drug
Drug Name: Mung Bean
Dosage Form: Intradermal; Subcutaneous Injection, Solution
Application #: BLA102223
Rev. Date: 


NDC Package Codes:

  • 49288-0044-1: 2 ML IN 1 VIAL, MULTI‑DOSE (49288‑0044‑1)
  • 49288-0044-2: 5 ML IN 1 VIAL, MULTI‑DOSE (49288‑0044‑2)
  • 49288-0044-3: 10 ML IN 1 VIAL, MULTI‑DOSE (49288‑0044‑3)
  • 49288-0044-4: 30 ML IN 1 VIAL, MULTI‑DOSE (49288‑0044‑4)
  • 49288-0044-5: 50 ML IN 1 VIAL, MULTI‑DOSE (49288‑0044‑5)

Active Ingredients:

  • Mung Bean

Dosage Strength:

  • .05 g/mL

Pharmaceutical Classes:

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

NDC QR Code

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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.