Nausea and Vomiting

• FDA approval · 2010-06-04
  FDA Approved: MECLIZINE HYDROCHLORIDE — Original Application (Jubilant Cadista Pharmacuticals Inc.)

  FDA approved the original application for meclizine hydrochloride from Jubilant Cadista Pharmaceuticals Inc., enabling a generic version of …

• FDA approval · 2010-06-03
  FDA Approved: METOCLOPRAMIDE — Supplemental Application (Teva Parenteral Medicines, Inc.)

  FDA approved a supplemental application for metoclopramide from Teva Parenteral Medicines, Inc., updating the product's approval status as p…

• FDA approval · 2010-03-31
  FDA Approved: METOCLOPRAMIDE — Supplemental Application (ANI Pharmaceuticals, Inc.)

  The FDA approved ANI Pharmaceuticals’ supplemental application for metoclopramide, updating the regulatory status of this generic drug.

• FDA approval · 2010-03-31
  FDA Approved: METOCLOPRAMIDE — Supplemental Application (Teva Pharmaceuticals USA, Inc.)

  FDA approved Teva Pharmaceuticals USA, Inc.'s supplemental application for metoclopramide (generic).

• FDA approval · 2009-08-18
  FDA Approved: CHLORPROMAZINE HYDROCHLORIDE — Supplemental Application (Upsher-Smith Laboratories, LLC)

  The FDA granted a supplemental approval for chlorpromazine hydrochloride from Upsher-Smith Laboratories, LLC.

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• FDA approval · 2009-07-15
  FDA Approved: PROCHLORPERAZINE MALEATE — Supplemental Application (Jubilant Cadista Pharmaceuticals Inc.)

  FDA approves a supplemental application for Prochlorperazine Maleate from Jubilant Cadista Pharmaceuticals Inc., granting approval for a gen…

• FDA approval · 2009-06-30
  FDA Approved: METOCLOPRAMIDE HYDROCHLORIDE — Supplemental Application (Chartwell Governmental & Specialty RX, LLC.)

  FDA approved a supplemental application for metoclopramide hydrochloride (generic), filed by Chartwell Governmental & Specialty RX, LLC., as…

• FDA approval · 2009-06-30
  FDA Approved: REGLAN — Supplemental Application (ANI Pharmaceuticals, Inc.)

  The FDA approved a supplemental application for Reglan (metoclopramide hydrochloride) submitted by ANI Pharmaceuticals, Inc. for NDA 017854.

• FDA approval · 2009-06-30
  FDA Approved: METOCLOPRAMIDE — Supplemental Application (ANI Pharmaceuticals, Inc.)

  The FDA approved ANI Pharmaceuticals' supplemental application for metoclopramide.

• FDA approval · 2009-06-29
  FDA Approved: PROCHLORPERAZINE — Supplemental Application (Cosette Pharmaceuticals, Inc.)

  FDA approved a supplemental application for Prochlorperazine from Cosette Pharmaceuticals, Inc., typically used to prevent nausea and vomiti…

• FDA approval · 2009-03-03
  FDA Approved: COMPRO — Supplemental Application (Padagis US LLC)

  The FDA approved a supplemental application for COMPRO (prochlorperazine) from Padagis US LLC.

• FDA approval · 2008-11-19
  FDA Approved: CHLORPROMAZINE HYDROCHLORIDE — Supplemental Application (Upsher-Smith Laboratories, LLC)

  FDA approved a supplemental application for chlorpromazine hydrochloride from Upsher-Smith Laboratories, approving changes to the approved d…

• FDA approval · 2008-06-12
  FDA Approved: METOCLOPRAMIDE — Original Application (Ipca Laboratories Limited)

  FDA approved the original generic application for metoclopramide by Ipca Laboratories Limited.

• FDA approval · 2008-05-15
  FDA Approved: COMPRO — Supplemental Application (Padagis US LLC)

  FDA approved a supplemental application for COMPRO (prochlorperazine) submitted by Padagis US LLC. This action updates the product’s approva…

• FDA approval · 2008-04-24
  FDA Approved: PROMETHAZINE HYDROCHLORIDE — Original Application (XGen Pharmaceuticals DJB, Inc.)

  The FDA approved the original ANDA for Promethazine hydrochloride (Promethazine HCl) from XGen Pharmaceuticals DJB, Inc. The approval covers…

• FDA approval · 2006-12-26
  FDA Approved: ONDANSETRON — Original Application (Hospira, Inc.)

  FDA approved Hospira's original application for ondansetron, a generic antiemetic used to prevent nausea and vomiting. The approval covers i…

• FDA approval · 2006-07-31
  FDA Approved: PROMETHAZINE HYDROCHLORIDE — Original Application (KVK-Tech, Inc.)

  The FDA approved KVK-Tech, Inc.'s original application for promethazine hydrochloride, establishing a generic product. This approval confirm…