22840-2329 : Firebush Kochia 40000 [Pnu]/Ml Intradermal; Percutaneous; Subcutaneous Solution


NDC: 22840-2329
Labeler: Greer Laboratories, Inc.
Product Type: Non-standardized Allergenic
Drug Name: Firebush Kochia
Dosage Form: Intradermal; Percutaneous; Subcutaneous Solution
Application #: BLA101833
Rev. Date: 


NDC Package Codes:

  • 22840-2329-2: 10 ML IN 1 VIAL, MULTI‑DOSE (22840‑2329‑2)
  • 22840-2329-4: 50 ML IN 1 VIAL, MULTI‑DOSE (22840‑2329‑4)

Active Ingredients:

  • Bassia Scoparia Pollen

Dosage Strength:

  • 40000 [PNU]/mL

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.
  • 22840-1325 Firebush Kochia .1 g/ml Intradermal; Percutaneous; Subcutaneous Solution by Greer Laboratories, Inc.
  • 22840-1326 Firebush Kochia .05 g/ml Intradermal; Percutaneous; Subcutaneous Solution by Greer Laboratories, Inc.
  • 22840-1327 Firebush Kochia 20000 [Pnu]/Ml Intradermal; Percutaneous; Subcutaneous Solution by Greer Laboratories, Inc.
  • 22840-1328 Firebush Kochia .001 g/ml Intradermal; Percutaneous; Subcutaneous Solution by Greer Laboratories, Inc.
  • 22840-5307 Firebush Kochia .05 g/ml Intradermal; Percutaneous; Subcutaneous Solution by Greer Laboratories, Inc.

NDC QR Code

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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.