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early humans
Generic Name: Secretin Synthetic Human
Date of Approval: April 9, 2004
Company: ChiRhoClin, Inc.
Treatment for: Secretin Stimulation Testing

The Food and Drug Administration, Center for Drug Evaluation and Research,Office of Drug Evaluation has issued ChiRhoClin, Inc early humans. an approval for HumanSecretin.
The FDA has approved three indications early humans. The indications of Human Secretin arethe following:

Stimulation of pancreatic secretions, including bicarbonate, to aid in thediagnosis of pancreatic exocrine dysfunction early humans.
Stimulation of gastrin secretion to aid in the diagnosis of gastrinoma, and
Stimulation of pancreatic secretion to facilitate the identification of theampulla of Vater and accessory papilla during endoscopic retrograde cholangiopancreatography(ERCP).
The FDA stated that they have completed the review of the NDA applications,as amended early humans. The FDA has concluded that adequate information has been presentedto demonstrate that the drug product is safe and effective for use as recommendedin the agreed upon indications.

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