0268-1139 : Populus Deltoides Ssp Monilifera Pollen .05 g/ml Subcutaneous Injection, Solution


NDC: 0268-1139
Labeler: Alk-abello, Inc.
Product Type: Non-standardized Allergenic
Drug Name: Populus Deltoides Ssp Monilifera Pollen
Dosage Form: Subcutaneous Injection, Solution
Application #: BLA103753
Rev. Date: 


NDC Package Codes:

  • 0268-1139-10: 10 ML IN 1 VIAL, MULTI‑DOSE (0268‑1139‑10)
  • 0268-1139-50: 50 ML IN 1 VIAL, MULTI‑DOSE (0268‑1139‑50)

Active Ingredients:

  • Populus Deltoides Subsp. Monilifera Pollen

Dosage Strength:

  • .05 g/mL

Pharmaceutical Classes:

  • Non-Standardized Pollen Allergenic Extract [EPC]
  • Increased Histamine Release [PE]
  • Cell-mediated Immunity [PE]
  • Increased IgG Production [PE]
  • Pollen [Chemical/Ingredient]
  • Allergens [Chemical/Ingredient]

Related Products:

Based on records with the same trade name.
  • 0268-1138 Populus Deltoides Ssp Monilifera Pollen .1 g/ml Subcutaneous Injection, Solution by Alk-abello, Inc.
  • 0268-6701 Populus Deltoides Ssp Monilifera Pollen .05 g/ml Percutaneous Injection, Solution by Alk-abello, Inc.
  • 0268-6702 Populus Deltoides Ssp Monilifera Pollen 1000 [pnu]/Ml Intradermal Injection, Solution by Alk-abello, 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.