49643-020 : Orris Root 1 g/10ml Cutaneous; Intradermal; Subcutaneous Injection


NDC49643-020
Labeler: Allermed Laboratories, Inc.
Product Type: Non-standardized Allergenic
Drug Name: Orris Root
Dosage Form: Cutaneous; Intradermal; Subcutaneous Injection
Application #: BLA102212
Rev. Date: 


NDC Package Codes:

  • 49643-020-05: 5 ML IN 1 VIAL, MULTI‑DOSE (49643‑020‑05)
  • 49643-020-10: 10 ML IN 1 VIAL, MULTI‑DOSE (49643‑020‑10)
  • 49643-020-30: 30 ML IN 1 VIAL, MULTI‑DOSE (49643‑020‑30)
  • 49643-020-50: 50 ML IN 1 VIAL, MULTI‑DOSE (49643‑020‑50)

Active Ingredients:

  • Iris Germanica Var. Florentina Root

Dosage Strength:

  • .1 g/mL

Pharmaceutical Classes:

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

Related Products:

Based on records with the same trade name.
  • 22840-1530 Orris Root .05 g/ml Intradermal; Percutaneous; Subcutaneous Solution by Greer Laboratories, Inc.
  • 22840-1531 Orris Root .001 g/ml Intradermal; Percutaneous; Subcutaneous Solution by Greer Laboratories, Inc.
  • 22840-5515 Orris Root .025 g/ml Intradermal; Percutaneous; Subcutaneous Solution by Greer Laboratories, Inc.
  • 36987-2234 Orris Root .05 g/ml Intradermal; Subcutaneous Injection, Solution by Nelco Laboratories, Inc.
  • 36987-2235 Orris Root .05 g/ml Intradermal; Subcutaneous Injection, Solution by Nelco Laboratories, Inc.
  • 36987-2236 Orris Root .1 g/ml Intradermal; Subcutaneous Injection, Solution by Nelco Laboratories, Inc.
  • 36987-2237 Orris Root .1 g/ml Intradermal; Subcutaneous Injection, Solution by Nelco Laboratories, Inc.
  • 49288-0343 Orris Root .1 g/ml Intradermal; Subcutaneous Injection, Solution by Antigen Laboratories, Inc.
  • 49288-0344 Orris Root .05 g/ml Intradermal; Subcutaneous Injection, Solution by Antigen Laboratories, Inc.
  • 54575-272 Orris Root 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.