0268-8062 : Mixed Shellfish Subcutaneous Injection, Solution


NDC0268-8062
Labeler: Alk-abello, Inc.
Product Type: Non-standardized Allergenic
Drug Name: Mixed Shellfish
Dosage Form: Subcutaneous Injection, Solution
Application #: BLA103753
Rev. Date: 


NDC Package Codes:

  • 0268-8062-10: 10.5 ML IN 1 VIAL (0268‑8062‑10)

Active Ingredients:

  • Crab Leg
  • Unspecified
  • Shrimp
  • Unspecified
  • Lobster
  • Unspecified
  • Oyster
  • Unspecified

Dosage Strength:

  • .1 g/mL
  • .1 g/mL
  • .1 g/mL
  • .1 g/mL

Pharmaceutical Classes:

  • Non-Standardized Food Allergenic Extract [EPC]
  • Increased Histamine Release [PE]
  • Cell-mediated Immunity [PE]
  • Allergens [CS]
  • Dietary Proteins [CS]
  • Shellfish Proteins [EXT]

Related Products:

Based on records with the same trade name.
  • 0268-8061 Mixed Shellfish Percutaneous Injection, Solution by Alk-abello, 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.