22840-2344 : Southern Ragweed .05 g/ml Intradermal; Percutaneous; Subcutaneous Solution


NDC: 22840-2344
Labeler: Greer Laboratories, Inc.
Product Type: Non-standardized Allergenic
Drug Name: Southern Ragweed
Dosage Form: Intradermal; Percutaneous; Subcutaneous Solution
Application #: BLA101833
Rev. Date: 


NDC Package Codes:

  • 22840-2344-2: 10 ML IN 1 VIAL, MULTI‑DOSE (22840‑2344‑2)

Active Ingredients:

  • Ambrosia Bidentata Pollen

Dosage Strength:

  • .05 g/mL

Pharmaceutical Classes:

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

Related Products:

Based on records with the same trade name.
  • 22840-1390 Southern Ragweed 20000 [Pnu]/Ml Intradermal; Percutaneous; Subcutaneous Solution by Greer Laboratories, Inc.
  • 22840-1392 Southern Ragweed .001 g/ml Intradermal; Percutaneous; Subcutaneous Solution by Greer Laboratories, Inc.
  • 22840-2345 Southern Ragweed .1 g/ml Intradermal; Percutaneous; Subcutaneous Solution by Greer Laboratories, Inc.
  • 22840-5327 Southern Ragweed .05 g/ml Intradermal; Percutaneous; Subcutaneous Solution by Greer Laboratories, Inc.
  • 49288-0449 Southern Ragweed .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.