22840-0202 : Standardized Kentucky (June) Bluegrass Pollen 100000 [Bau]/Ml Intradermal; Percutaneous; Subcutaneous Solution


NDC: 22840-0202
Labeler: Greer Laboratories, Inc.
Product Type: Standardized Allergenic
Drug Name: Standardized Kentucky (June) Bluegrass Pollen
Dosage Form: Intradermal; Percutaneous; Subcutaneous Solution
Application #: BLA101837
Rev. Date: 


NDC Package Codes:

  • 22840-0202-2: 10 ML IN 1 VIAL, MULTI‑DOSE (22840‑0202‑2)
  • 22840-0202-4: 50 ML IN 1 VIAL, MULTI‑DOSE (22840‑0202‑4)
  • 22840-0202-5: 5 ML IN 1 BOTTLE, DROPPER (22840‑0202‑5)

Active Ingredients:

  • Poa Pratensis Pollen

Dosage Strength:

  • 100000 [BAU]/mL

Pharmaceutical Classes:

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

Related Products:

Based on records with the same trade name.
  • 22840-0201 Standardized Kentucky (June) Bluegrass Pollen 10000 [Bau]/Ml Intradermal; Percutaneous; Subcutaneous Solution by Greer Laboratories, Inc.
  • 36987-2427 Standardized Kentucky (June) Bluegrass Pollen 100000 [bau]/Ml Intradermal; Subcutaneous Injection, Solution by Nelco Laboratories, Inc.
  • 36987-2428 Standardized Kentucky (June) Bluegrass Pollen 10000 [bau]/Ml Intradermal; Subcutaneous Injection, Solution by Nelco 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.