49288-0038 : Botrytis .1 g/ml Intradermal; Subcutaneous Injection, Solution


NDC: 49288-0038
Labeler: Antigen Laboratories, Inc.
Product Type: Human Prescription Drug
Drug Name: Botrytis
Dosage Form: Intradermal; Subcutaneous Injection, Solution
Application #: BLA102223
Rev. Date: 


NDC Package Codes:

  • 49288-0038-1: 2 ML IN 1 VIAL, MULTI‑DOSE (49288‑0038‑1)
  • 49288-0038-2: 5 ML IN 1 VIAL, MULTI‑DOSE (49288‑0038‑2)
  • 49288-0038-3: 10 ML IN 1 VIAL, MULTI‑DOSE (49288‑0038‑3)
  • 49288-0038-4: 30 ML IN 1 VIAL, MULTI‑DOSE (49288‑0038‑4)
  • 49288-0038-5: 50 ML IN 1 VIAL, MULTI‑DOSE (49288‑0038‑5)

Active Ingredients:

  • Botrytis Cinerea

Dosage Strength:

  • .1 g/mL

Pharmaceutical Classes:

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

Related Products:

Based on records with the same trade name.
  • 49288-0039 Botrytis .05 g/ml Intradermal; Subcutaneous Injection, Solution by Antigen Laboratories, Inc.
  • 49643-104 Botrytis 1 g/10ml 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.