36987-1421 : Brussels Sprout .1 g/ml Intradermal; Subcutaneous Injection, Solution


NDC: 36987-1421
Labeler: Nelco Laboratories, Inc.
Product Type: Human Prescription Drug
Drug Name: Brussels Sprout
Dosage Form: Intradermal; Subcutaneous Injection, Solution
Application #: BLA102192
Rev. Date: 


NDC Package Codes:

  • 36987-1421-1: 5 ML IN 1 VIAL, MULTI‑DOSE (36987‑1421‑1)
  • 36987-1421-2: 10 ML IN 1 VIAL, MULTI‑DOSE (36987‑1421‑2)
  • 36987-1421-3: 30 ML IN 1 VIAL, MULTI‑DOSE (36987‑1421‑3)
  • 36987-1421-4: 50 ML IN 1 VIAL, MULTI‑DOSE (36987‑1421‑4)

Active Ingredients:

  • Brussels Sprout

Dosage Strength:

  • .1 g/mL

Pharmaceutical Classes:

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

Related Products:

Based on records with the same trade name.
  • 36987-1418 Brussels Sprout .05 g/ml Intradermal; Subcutaneous Injection, Solution by Nelco Laboratories, Inc.
  • 36987-1419 Brussels Sprout .05 g/ml Intradermal; Subcutaneous Injection, Solution by Nelco Laboratories, Inc.
  • 36987-1420 Brussels Sprout .1 g/ml Intradermal; Subcutaneous Injection, Solution by Nelco Laboratories, Inc.
  • 49288-0050 Brussels Sprout .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.