Bynfezia Pen

Active Ingredient(s): Octreotide Acetate
FDA Approved: * January 28, 2020
Pharm Company: * SUN PHARM
Category: Cancer

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

Bynfezia Pen Overview

Octreotide, sold under the brand name Sandostatin among others, is an octapeptide that mimics natural somatostatin pharmacologically, though it is a more potent inhibitor of growth hormone, glucagon, and insulin than the natural hormone. It was first synthesized in 1979 by the chemist Wilfried Bauer, and binds predominantly to the somatostatin receptors SSTR2 and SSTR5.[3] It was approved for use in the United States in 1988.[2][1] Contents 1 ...

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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:

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Possible Dosages for this and Related Drugs:

Octreotide Acetate
  • Capsule, Delayed Release: 20mg
  • Injection: 0.05mg/ml, 0.1mg/ml, 0.2mg/ml, 0.5mg/ml, 1000mcg/ml, 100mcg/ml, 10mg, 1mg/ml, 200mcg/ml, 20mg, 30mg, 500mcg/ml, 50mcg/ml
  • Solution: 2.5mg/ml (2.5mg/ml)
Note: Above list includes dosages for all drugs with the same combination of active ingredients.

NDC Database Records for Bynfezia Pen: (1 result)

Sorted by National Drug Code
  • 62756-452 Bynfezia Pen 2.5 mg/ml Subcutaneous Injection by Sun Pharmaceutical Industries, Inc.

Other drugs which contain Octreotide Acetate or a similar ingredient: (4 results)

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