Duodenal Ulcer

• FDA approval · 2006-10-20
  FDA Approved: NEXIUM — Original Application (AstraZeneca Pharmaceuticals LP)

  FDA approved Nexium (esomeprazole magnesium) as AstraZeneca's original NDA. The approval established Nexium as a proton pump inhibitor for a…

• FDA approval · 2006-10-13
  FDA Approved: RANITIDINE — Original Application (Amneal Pharmaceuticals of New York LLC)

  The FDA approved Amneal Pharmaceuticals of New York LLC's original application for generic ranitidine, authorizing its commercial ranitidine…

• FDA approval · 2006-09-26
  FDA Approved: OMEPRAZOLE — Supplemental Application (Lannett Company, Inc.)

  FDA approved a supplemental application for omeprazole from Lannett Company, Inc., enabling the marketing of the generic omeprazole product.

• FDA approval · 2006-09-25
  FDA Approved: FAMOTIDINE — Original Application (Chain Drug Consortium, LLC)

  The FDA approved Chain Drug Consortium, LLC's original application for famotidine, enabling a generic version of famotidine to be marketed. …

• FDA approval · 2006-09-25
  FDA Approved: ACID RELIEF — Original Application (Rite Aid Corporation)

  The FDA approved ACID RELIEF (famotidine) from Rite Aid under an Original Application (ANDA), making a generic famotidine product available.

• Want full summaries, importance scores, and drug timelines? Upgrade to Plus or Pro.
• FDA approval · 2006-07-25
  FDA Approved: PROTONIX DELAYED-RELEASE — Supplemental Application (Wyeth Pharmaceuticals LLC, a subsidiary of Pfizer Inc.)

  The FDA approved a supplemental application for Protonix Delayed-Release (pantoprazole sodium) submitted by Wyeth Pharmaceuticals LLC, a sub…

• FDA approval · 2006-06-09
  FDA Approved: PEPCID AC MAXIMUM STRENGTH — Supplemental Application (Kenvue Brands LLC)

  FDA approved a supplemental application for Pepcid AC Maximum Strength (famotidine) by Kenvue Brands LLC, supporting a higher-strength formu…