0268-1064 : Betula Nigra Pollen 10000 [pnu]/Ml Subcutaneous Injection, Solution


NDC: 0268-1064
Labeler: Alk-abello, Inc.
Product Type: Non-standardized Allergenic
Drug Name: Betula Nigra Pollen
Dosage Form: Subcutaneous Injection, Solution
Application #: BLA103753
Rev. Date: 


NDC Package Codes:

  • 0268-1064-50: 50 ML IN 1 VIAL, MULTI‑DOSE (0268‑1064‑50)

Active Ingredients:

  • Betula Nigra Pollen

Dosage Strength:

  • 10000 [PNU]/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.
  • 0268-1062 Betula Nigra Pollen .1 g/ml Subcutaneous Injection, Solution by Alk-abello, Inc.
  • 0268-1063 Betula Nigra Pollen .05 g/ml Subcutaneous Injection, Solution by Alk-abello, Inc.
  • 0268-1065 Betula Nigra Pollen 20000 [pnu]/Ml Subcutaneous Injection, Solution by Alk-abello, Inc.
  • 0268-1066 Betula Nigra Pollen 40000 [pnu]/Ml Subcutaneous Injection, Solution by Alk-abello, Inc.
  • 0268-6609 Betula Nigra Pollen .05 g/ml Percutaneous Injection, Solution by Alk-abello, Inc.
  • 0268-6687 Betula Nigra 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.