54575-131 : Nettle Pollen 1 g/20ml Percutaneous; Subcutaneous Injection, Solution


NDC: 54575-131
Labeler: Allergy Laboratories, Inc.
Product Type: Human Prescription Drug
Drug Name: Nettle Pollen
Dosage Form: Percutaneous; Subcutaneous Injection, Solution
Application #: BLA101376
Rev. Date: 


NDC Package Codes:

  • 54575-131-02: 2 ML IN 1 VIAL, MULTI‑DOSE (54575‑131‑02)
  • 54575-131-10: 10 ML IN 1 VIAL, MULTI‑DOSE (54575‑131‑10)
  • 54575-131-30: 30 ML IN 1 VIAL, MULTI‑DOSE (54575‑131‑30)
  • 54575-131-50: 50 ML IN 1 VIAL, MULTI‑DOSE (54575‑131‑50)

Active Ingredients:

  • Urtica Dioica Pollen

Dosage Strength:

  • 1 g/20mL

Pharmaceutical Classes:

  • Non-Standardized Pollen Allergenic Extract [EPC]
  • Increased Histamine Release [PE]
  • Cell-mediated Immunity [PE]
  • Increased IgG Production [PE]
  • Pollen [CS]
  • Allergens [CS]

Related Products:

Based on records with the same trade name.
  • 49288-0330 Nettle Pollen .05 g/ml Intradermal; Subcutaneous Injection, Solution by Antigen Laboratories, Inc.
  • 49643-423 Nettle Pollen 1 g/20ml Cutaneous; Intradermal; Subcutaneous Injection by Allermed 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.