0268-1072 : Betula Lenta Pollen .0005 g/ml Subcutaneous Injection, Solution


NDC: 0268-1072
Labeler: Alk-abello, Inc.
Product Type: Non-standardized Allergenic
Drug Name: Betula Lenta Pollen
Dosage Form: Subcutaneous Injection, Solution
Application #: BLA103753
Rev. Date: 


NDC Package Codes:

  • 0268-1072-50: 50 ML IN 1 VIAL, MULTI‑DOSE (0268‑1072‑50)

Active Ingredients:

  • Betula Lenta Pollen

Dosage Strength:

  • .0005 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.
  • 0268-1056 Betula Lenta Pollen .1 g/ml Subcutaneous Injection, Solution by Alk-abello, Inc.
  • 0268-1057 Betula Lenta Pollen 40000 [pnu]/Ml Subcutaneous Injection, Solution by Alk-abello, Inc.
  • 0268-1058 Betula Lenta Pollen .05 g/ml Subcutaneous Injection, Solution by Alk-abello, Inc.
  • 0268-1059 Betula Lenta Pollen 50000 [pnu]/Ml Subcutaneous Injection, Solution by Alk-abello, Inc.
  • 0268-1069 Betula Lenta Pollen .1 g/ml Subcutaneous Injection, Solution by Alk-abello, Inc.
  • 0268-1070 Betula Lenta Pollen .05 g/ml Subcutaneous Injection, Solution by Alk-abello, Inc.
  • 0268-1071 Betula Lenta Pollen .005 g/ml Subcutaneous Injection, Solution by Alk-abello, Inc.
  • 0268-1073 Betula Lenta Pollen 40000 [pnu]/Ml Subcutaneous Injection, Solution by Alk-abello, Inc.
  • 0268-6608 Betula Lenta Pollen .05 g/ml Percutaneous Injection, Solution by Alk-abello, Inc.
  • 0268-6610 Betula Lenta Pollen .05 g/ml Percutaneous Injection, Solution by Alk-abello, Inc.
  • 0268-6686 Betula Lenta Pollen 1000 [pnu]/Ml Intradermal Injection, Solution by Alk-abello, Inc.
  • 0268-6688 Betula Lenta Pollen 1000 [pnu]/Ml Intradermal Injection, Solution by Alk-abello, Inc.
  • 0268-6772 Betula Lenta Pollen .002 g/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.