Allergic Conjunctivitis

• FDA approval · 2009-04-30
  FDA Approved: AZELASTINE HYDROCHLORIDE — Original Application (Apotex Corp.)

  FDA approved Apotex Corp.'s original application for azelastine hydrochloride, a generic antihistamine product.

• FDA approval · 2009-04-27
  FDA Approved: CETIRIZINE HYDROCHLORIDE ORAL SOLUTION — Original Application (APOZEAL PHARMACEUTICALS INC)

  FDA approved Apozeal Pharmaceuticals' cetirizine hydrochloride oral solution as an original generic product.

• FDA approval · 2008-09-02
  FDA Approved: ZADITOR — Original Application (Alcon Laboratories, Inc.)

  The FDA approved Alcon's ketotifen fumarate ophthalmic solution as a generic product under ANDA 077200 (brand name Zaditor).

• FDA approval · 2008-07-07
  FDA Approved: ALOCRIL — Supplemental Application (Allergan, Inc.)

  FDA approved a supplemental application for ALOCRIL (nedocromil sodium) from Allergan to update its labeling for allergic conjunctivitis.

• FDA approval · 2007-12-28
  FDA Approved: CETIRIZINE HCL — Original Application (GLENMARK THERAPEUTICS INC., USA)

  FDA approved Glenmark's cetirizine HCl Original Application (ANDA), granting marketing rights for a generic cetirizine product. Indications …

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• FDA approval · 2007-10-18
  FDA Approved: XYZAL — Supplemental Application (Chattem, Inc.)

  The FDA approved a supplemental application for XYZAL (levocetirizine dihydrochloride) submitted by Chattem, Inc.

• FDA approval · 2007-08-21
  FDA Approved: ALOCRIL — Supplemental Application (Allergan, Inc.)

  The FDA approved Allergan's supplemental application for ALOCRIL (nedocromil sodium) submitted by Allergan, Inc.

• FDA approval · 2007-07-31
  FDA Approved: EYE ALLERGY RELIEF — Supplemental Application (DOLGENCORP, LLC)

  FDA approved a supplemental application for Eye Allergy Relief containing pheniramine maleate and naphaZoline hydrochloride, manufactured by…

• FDA approval · 2007-07-26
  FDA Approved: KETOTIFEN FUMARATE OPHTHALMIC SOLUTION — Original Application (Sentiss Pharmaceuticals LLC)

  The FDA approved Ketotifen Fumarate Ophthalmic Solution as an original-application (ANDA) product from Sentiss Pharmaceuticals LLC for the t…

• FDA approval · 2007-04-26
  FDA Approved: PATADAY ONCE DAILY RELIEF — Supplemental Application (Alcon Laboratories, Inc.)

  FDA supplemental approval granted for Pataday Once Daily Relief with olopatadine hydrochloride, expanding labeling for once-daily dosing in …

• FDA approval · 2006-12-01
  FDA Approved: EYE ITCH RELIEF — Original Application (Target Corporation)

  FDA approved Eye Itch Relief from Target Corporation via an Original Application NDA for ketotifen fumarate eye drops, indicated for relief …

• FDA approval · 2006-10-04
  FDA Approved: PATADAY ONCE DAILY RELIEF — Supplemental Application (Alcon Laboratories, Inc.)

  FDA approved a supplemental application for Pataday Once Daily Relief (olopatadine hydrochloride) by Alcon Laboratories, expanding the label…

• 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…