Hypertension

• FDA approval · 2011-10-27
  FDA Approved: AMLODIPINE BESYLATE AND BENAZEPRIL HYDROCHLORIDE — Supplemental Application (Dr.Reddy's Laboratories Limited)

  FDA approved a supplemental application for Amlodipine Besylate and Benazepril Hydrochloride by Dr. Reddy's Laboratories Limited.

• FDA approval · 2011-10-26
  FDA Approved: LOSARTAN POTASSIUM AND HYDROCHLOROTHIAZIDE — Supplemental Application (NorthStar Rx LLC)

  The FDA approved a supplemental application for losartan potassium and hydrochlorothiazide from NorthStar Rx LLC. Losartan potassium and hyd…

• FDA approval · 2011-10-25
  FDA Approved: ATENOLOL — Supplemental Application (Teva Pharmaceuticals USA, Inc.)

  FDA approved a supplemental application for Atenolol from Teva Pharmaceuticals USA, Inc. This action updates the regulatory status of the ge…

• FDA approval · 2011-10-18
  FDA Approved: ATENOLOL — Supplemental Application (Aurobindo Pharma Limited)

  The FDA approved a supplemental application for atenolol submitted by Aurobindo Pharma Limited, granting regulatory approval for the supplem…

• FDA approval · 2011-10-17
  FDA Approved: PERINDOPRIL ERBUMINE — Supplemental Application (Aurobindo Pharma Limited)

  FDA approved a supplemental application for PERINDOPRIL ERBUMINE from Aurobindo Pharma Limited (ANDA) to market the generic product.

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• FDA approval · 2011-10-13
  FDA Approved: HYDROCHLOROTHIAZIDE — Supplemental Application (Unichem Pharmaceuticals (USA), Inc.)

  The FDA approved a supplemental application for hydrochlorothiazide from Unichem Pharmaceuticals (USA), Inc., approving a generic hydrochlor…

• FDA approval · 2011-10-12
  FDA Approved: ALISKIREN — Supplemental Application (Prasco Laboratories)

  FDA approved a supplemental application for aliskiren hemifumarate from Prasco Laboratories.

• FDA approval · 2011-09-27
  FDA Approved: PROCARDIA XL — Supplemental Application (Pfizer Laboratories Div Pfizer Inc)

  FDA approved a supplemental application for PROCARDIA XL (nifedipine) from Pfizer Laboratories Div Pfizer Inc.

• FDA approval · 2011-09-22
  FDA Approved: SPIRONOLACTONE AND HYDROCHLOROTHIAZIDE — Supplemental Application (Prasco Laboratories)

  FDA approves a supplemental application for the spironolactone and hydrochlorothiazide combination from Prasco Laboratories. This action upd…

• FDA approval · 2011-09-21
  FDA Approved: TORSEMIDE — Supplemental Application (Teva Pharmaceuticals USA, Inc.)

  FDA approved a supplemental application for torsemide from Teva Pharmaceuticals USA, Inc. This approval pertains to a supplemental submissio…

• FDA approval · 2011-09-21
  FDA Approved: BENAZEPRIL HYDROCHLORIDE — Supplemental Application (Aurobindo Pharma Limited)

  FDA approved a supplemental application for benazepril hydrochloride from Aurobindo Pharma Limited under the ANDA program.

• FDA approval · 2011-09-13
  FDA Approved: ATENOLOL — Supplemental Application (Zydus Lifesciences Limited)

  FDA approves a supplemental application for Atenolol by Zydus Lifesciences Limited under an ANDA, authorizing an approved supplemental actio…

• FDA approval · 2011-08-31
  FDA Approved: AMLODIPINE BESYLATE — Supplemental Application (Aurobindo Pharma Limited)

  The FDA approved a supplemental application for amlodipine besylate from Aurobindo Pharma Limited, authorizing continued marketing of the ge…

• FDA approval · 2011-08-31
  FDA Approved: AMLODIPINE BESYLATE AND BENAZEPRIL HYDROCHLORIDE — Supplemental Application (Lupin Pharmaceuticals, Inc.)

  The FDA approved Lupin's supplemental application for a generic fixed-dose combination of amlodipine besylate and benazepril hydrochloride f…

• FDA approval · 2011-08-31
  FDA Approved: AMLODIPINE BESYLATE AND BENAZEPRIL HYDROCHLORIDE — Supplemental Application (Dr.Reddy's Laboratories Limited)

  The FDA approved a supplemental application for a generic fixed-dose combination of amlodipine besylate and benazepril hydrochloride (Dr. Re…

• FDA approval · 2011-08-29
  FDA Approved: BISOPROLOL FUMARATE — Supplemental Application (TruPharma LLC)

  The FDA approved a supplemental application for bisoprolol fumarate by TruPharma LLC, under an ANDA.

• FDA approval · 2011-08-29
  FDA Approved: BISOPROLOL FUMARATE AND HYDROCHLOROTHIAZIDE — Supplemental Application (Unichem Pharmaceuticals (USA), Inc.)

  FDA approved a supplemental application for the generic fixed-dose combination of bisoprolol fumarate and hydrochlorothiazide from Unichem P…

• FDA approval · 2011-08-29
  FDA Approved: BISOPROLOL FUMARATE — Supplemental Application (NorthStar Rx LLC)

  FDA approved NorthStar Rx LLC's supplemental application for bisoprolol fumarate, confirming approval of a generic product. The approval per…

• FDA approval · 2011-08-26
  FDA Approved: HYZAAR — Supplemental Application (Organon LLC)

  The FDA approved a supplemental application for HYZAAR (losartan potassium and hydrochlorothiazide) submitted by Organon LLC.

• FDA approval · 2011-08-21
  FDA Approved: TENORETIC — Supplemental Application (Upsher-Smith Laboratories, LLC)

  FDA approved a supplemental application for Tenoretic (atenolol and chlorthalidone) from Upsher-Smith Laboratories, LLC. The approval pertai…

• FDA approval · 2011-08-19
  FDA Approved: DILTIAZEM HYDROCHLORIDE — Supplemental Application (OCEANSIDE PHARMACEUTICALS)

  FDA approved Oceanside Pharmaceuticals' supplemental application for diltiazem hydrochloride, allowing continued marketing of this generic p…

• FDA approval · 2011-08-17
  FDA Approved: TENORMIN — Supplemental Application (Almatica Pharma LLC)

  FDA approved a supplemental application for Tenormin (atenolol) from Almatica Pharma LLC.

• FDA approval · 2011-08-17
  FDA Approved: HYDROCHLOROTHIAZIDE — Supplemental Application (Alembic Pharmaceuticals Limited)

  FDA approved a supplemental application for Hydrochlorothiazide from Alembic Pharmaceuticals Limited, adding a generic version of the diuret…

• FDA approval · 2011-08-04
  FDA Approved: ZESTORETIC — Supplemental Application (Almatica Pharma Inc.)

  The FDA has approved a supplemental application for ZESTORETIC (lisinopril and hydrochlorothiazide) submitted by Almatica Pharma Inc. This a…

• FDA approval · 2011-08-03
  FDA Approved: VERAPAMIL HYDROCHLORIDE — Original Application (Glenmark Pharmaceuticals Inc., USA)

  FDA approved verapamil hydrochloride as an original application generic drug by Glenmark; the product is indicated for conditions treated by…