49288-0051 : Buckwheat .05 g/ml Intradermal; Subcutaneous Injection, Solution


NDC49288-0051
Labeler: Antigen Laboratories, Inc.
Product Type: Human Prescription Drug
Drug Name: Buckwheat
Dosage Form: Intradermal; Subcutaneous Injection, Solution
Application #: BLA102223
Rev. Date: 


NDC Package Codes:

  • 49288-0051-1: 2 ML IN 1 VIAL, MULTI‑DOSE (49288‑0051‑1)
  • 49288-0051-2: 5 ML IN 1 VIAL, MULTI‑DOSE (49288‑0051‑2)
  • 49288-0051-3: 10 ML IN 1 VIAL, MULTI‑DOSE (49288‑0051‑3)
  • 49288-0051-4: 30 ML IN 1 VIAL, MULTI‑DOSE (49288‑0051‑4)
  • 49288-0051-5: 50 ML IN 1 VIAL, MULTI‑DOSE (49288‑0051‑5)

Active Ingredients:

  • Buckwheat

Dosage Strength:

  • .05 g/mL

Pharmaceutical Classes:

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

Related Products:

Based on records with the same trade name.
  • 0268-6113 Buckwheat .1 g/ml Percutaneous Injection, Solution by Alk-abello, Inc.
  • 22840-5709 Buckwheat .05 g/ml Intradermal; Percutaneous; Subcutaneous Solution by Greer Laboratories, Inc.
  • 54575-358 Buckwheat 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.