22840-5784 : Coconut .05 g/ml Intradermal; Percutaneous; Subcutaneous Solution


NDC: 22840-5784
Labeler: Greer Laboratories, Inc.
Product Type: Non-standardized Allergenic
Drug Name: Coconut
Dosage Form: Intradermal; Percutaneous; Subcutaneous Solution
Application #: BLA101833
Rev. Date: 


NDC Package Codes:

  • 22840-5784-2: 10 ML IN 1 VIAL, MULTI‑DOSE (22840‑5784‑2)
  • 22840-5784-5: 5 ML IN 1 BOTTLE, DROPPER (22840‑5784‑5)

Active Ingredients:

  • Coconut

Dosage Strength:

  • .05 g/mL

Pharmaceutical Classes:

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

Related Products:

Based on records with the same trade name.
  • 0268-6127 Coconut .1 g/ml Percutaneous Injection, Solution by Alk-abello, Inc.
  • 36987-1538 Coconut .05 g/ml Intradermal; Subcutaneous Injection, Solution by Nelco Laboratories, Inc.
  • 36987-1539 Coconut .05 g/ml Intradermal; Subcutaneous Injection, Solution by Nelco Laboratories, Inc.
  • 36987-1540 Coconut .1 g/ml Intradermal; Subcutaneous Injection, Solution by Nelco Laboratories, Inc.
  • 36987-1541 Coconut .1 g/ml Intradermal; Subcutaneous Injection, Solution by Nelco Laboratories, Inc.
  • 49288-0120 Coconut .05 g/ml Intradermal; Subcutaneous Injection, Solution by Antigen Laboratories, Inc.
  • 54575-378 Coconut 1 g/20ml Percutaneous; Subcutaneous Injection, Solution by Allergy Laboratories, 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.