18657-102 : Hylenex Recombinant 150 [usp'u]/Ml Subcutaneous Injection, Solution


NDC18657-102
Labeler: Halozyme, Inc.
Product Type: Human Prescription Drug
Drug Name:  Hylenex Recombinant
Dosage Form: Subcutaneous Injection, Solution
Application #: NDA021859
Rev. Date: 


NDC Package Codes:

  • 18657-102-04: 4 BOX IN 1 CARTON (18657‑102‑04) > 1 VIAL IN 1 BOX (18657‑102‑02) > 1 ML IN 1 VIAL (18657‑102‑01)
  • 18657-102-10: 10 BOX IN 1 CARTON (18657‑102‑10) > 1 VIAL IN 1 BOX (18657‑102‑02) > 1 ML IN 1 VIAL (18657‑102‑01)

Active Ingredients:

  • Hyaluronidase (Human Recombinant)

Dosage Strength:

  • 150 [USP'U]/mL

Pharmaceutical Classes:

  • Endoglycosidase [EPC]
  • Glycoside Hydrolases [Chemical/Ingredient]

Related Products:

Based on records with the same trade name.
  • 18657-117 Hylenex Recombinant 150 [usp'u]/Ml Subcutaneous Injection, Solution by Halozyme, Inc.
  • 50090-4534 Hylenex Recombinant 150 [Usp'u]/Ml Subcutaneous Injection, Solution by A-s Medication Solutions
  • 60977-319 Hylenex Recombinant 150 [usp'u]/Ml Subcutaneous Injection, Solution by Baxter Healthcare Corporation

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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.