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FDA approval · 2020-11-30

FDA Approved: LUBIPROSTONE — Supplemental Application (Dr. Reddy's Laboratories Inc.)

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Summary

The FDA approved a supplemental application for Lubiprostone submitted by Dr. Reddy's Laboratories, updating labeling under NDA 021908.

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Diseases / indications

Drugs mentioned

  • LUBIPROSTONE (lubiprostone)

Snippet

SUPPL AP for LUBIPROSTONE (LUBIPROSTONE)