Hylenex Recombinant

Active Ingredient(s): Hyaluronidase Recombinant Human
FDA Approved: * December 2, 2005
Pharm Company: * HALOZYME THERAP
Category: Medical Device

* This drug may consist of multiple approval dates, manufacturers, or distributors. If applicable, they would be listed below under "NDC Database Records".

Hylenex Recombinant Overview

Hyaluronidases are a family of enzymes that catalyse the degradation of hyaluronic acid (HA). Karl Meyer classified these enzymes in 1971, into three distinct groups, a scheme based on the enzyme reaction products.[1] The three main types of hyaluronidases are two classes of eukaryotic endoglycosidase hydrolases and a prokaryotic lyase-type of glycosidase.[2] In humans, there are five functional hyaluronidases: HYAL1, HYAL2, HYAL3, HYAL4 and HYAL5 (also known a...

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Details May Include Instructions, Side Effects, Interactions, Etc. Drug monograph is from Wikipedia. All text is available under the terms of the GFDL (GNU Free Documentation License). Source: en.wikipedia.org/wiki/Hyaluronidase

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Possible Dosages for this and Related Drugs:

Hyaluronidase Recombinant Human
  • Injection: 1,500 units/vial, 150 units/ml, 150 units/vial, 150unit/ml, 150USPunits/ml, 200 units/vial, 200units/ml, 6,200 units/vial
  • Powder for Reconstitution: 6200IU/5ml
Note: Above list includes dosages for all drugs with the same combination of active ingredients.

NDC Database Records for Hylenex Recombinant: (4 results)

Sorted by National Drug Code
  • 18657-102 Hylenex Recombinant 150 [usp'u]/Ml Subcutaneous Injection, Solution by Halozyme, Inc.
  • 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

Other drugs which contain Hyaluronidase Recombinant Human or a similar ingredient: (5 results)

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