Supraventricular Tachycardia

• FDA approval · 2026-04-10
  FDA Approved: DILTIAZEM HYDROCHLORIDE — Supplemental Application (ScieGen Pharmaceuticals, Inc.)

  The FDA approved a supplemental application for diltiazem hydrochloride from ScieGen Pharmaceuticals, Inc.

• FDA approval · 2026-02-27
  FDA Approved: DILTIAZEM HYDROCHLORIDE — Original Application (Macleods Pharmaceuticals Limited)

  FDA approved the original abbreviated new drug application for diltiazem hydrochloride from Macleods Pharmaceuticals Limited.

• FDA approval · 2026-02-23
  FDA Approved: DILTIAZEM HYDROCHLORIDE — Supplemental Application (Zydus Pharmaceuticals (USA) Inc.)

  The FDA approved a supplemental application for diltiazem hydrochloride from Zydus Pharmaceuticals USA Inc., approving a generic product.

• FDA approval · 2026-02-09
  FDA Approved: DIGOXIN — Supplemental Application (Amneal Pharmaceuticals of New York LLC)

  FDA approved a supplemental application for Digoxin submitted by Amneal Pharmaceuticals of New York LLC.

• FDA approval · 2025-11-14
  FDA Approved: DILTIAZEM HYDROCHLORIDE — Original Application (Alembic Pharmaceuticals Limited)

  FDA approves the original application for diltiazem hydrochloride (Alembic Pharmaceuticals Limited), a generic product, for use in treating …

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• FDA approval · 2025-09-19
  FDA Approved: VERAPAMIL HYDROCHLORIDE — Supplemental Application (Amneal Pharmaceuticals LLC)

  FDA approved a supplemental application for verapamil hydrochloride from Amneal Pharmaceuticals LLC under ANDA210994. This approval authoriz…

• FDA approval · 2025-09-11
  FDA Approved: DILTIAZEM HYDROCHLORIDE — Supplemental Application (Actavis Pharma, Inc.)

  FDA approved a supplemental application for diltiazem hydrochloride from Actavis Pharma, Inc., confirming/expanding the product's regulatory…

• FDA approval · 2025-07-02
  FDA Approved: DILTIAZEM HYDROCHLORIDE — Original Application (Ingenus Pharmaceuticals, LLC)

  FDA approved a generic diltiazem hydrochloride product from Ingenus Pharmaceuticals under an Original Application (ANDA), expanding access t…

• FDA approval · 2025-04-16
  FDA Approved: DILTIAZEM HYDROCHLORIDE EXTENDED RELEASE — Supplemental Application (Oceanside Pharmaceuticals)

  The FDA approved Oceanside Pharmaceuticals' supplemental NDA for the extended-release form of diltiazem hydrochloride.

• FDA approval · 2025-04-16
  FDA Approved: DILTIAZEM HYDROCHLORIDE — Supplemental Application (Oceanside Pharmaceuticals)

  FDA approved a supplemental application for diltiazem hydrochloride by Oceanside Pharmaceuticals.

• FDA approval · 2025-02-21
  FDA Approved: NEXTERONE — Supplemental Application (Baxter Healthcare Company)

  The FDA approved a supplemental application for NEXTERONE (amiodarone hydrochloride) from Baxter Healthcare Company.

• FDA approval · 2025-02-21
  FDA Approved: DILTIAZEM HYDROCHLORIDE IN SODIUM CHLORIDE — Original Application (WG Critical Care, LLC)

  FDA approved a new injectable diltiazem hydrochloride in sodium chloride under an original NDA from WG Critical Care, LLC. This parenteral f…

• FDA approval · 2024-10-18
  FDA Approved: DILTIAZEM HYDROCHLORIDE — Original Application (Alembic Pharmaceuticals Inc.)

  FDA approved Alembic Pharmaceuticals' generic diltiazem hydrochloride under an Original Application (ANDA).

• FDA approval · 2024-10-17
  FDA Approved: PROPAFENONE HYDROCHLORIDE — Supplemental Application (Strides Pharma Science Limited)

  The FDA approved a supplemental application for Propafenone Hydrochloride filed by Strides Pharma Science Limited, adding a approved generic…

• FDA approval · 2024-10-15
  FDA Approved: ESMOLOL HYDROCHLORIDE — Supplemental Application (Amneal Pharmaceuticals LLC)

  FDA supplemental approval for Amneal's esmolol hydrochloride in sodium chloride, a generic injectable product.

• FDA approval · 2024-09-09
  FDA Approved: VERAPAMIL HYDROCHLORIDE — Supplemental Application (Hospira, Inc.)

  FDA approved a supplemental application for Verapamil Hydrochloride (Hospira, Inc.), confirming it as an approved generic drug under an ANDA…

• FDA approval · 2024-07-09
  FDA Approved: ESMOLOL HYDROCHLORIDE — Supplemental Application (Eugia US LLC)

  The FDA approved a supplemental application for esmolol hydrochloride from Eugia US LLC, authorizing changes to the approved product under a…

• FDA approval · 2024-07-09
  FDA Approved: ESMOLOL HYDROCHLORIDE — Supplemental Application (Eugia US LLC)

  The FDA approved a supplemental application for esmolol hydrochloride in sodium chloride (Esmolol Hydrochloride in Sodium Chloride) filed by…

• FDA approval · 2023-03-07
  FDA Approved: DILTIAZEM HYDROCHLORIDE — Original Application (Slate Run Pharmaceuticals, LLC)

  FDA approved Slate Run Pharmaceuticals, LLC's generic diltiazem hydrochloride through an original ANDA.

• FDA approval · 2023-03-01
  FDA Approved: DILTIAZEM HYDROCHLORIDE — Original Application (Upsher-Smith Laboratories, LLC)

  FDA approved Upsher-Smith's generic diltiazem hydrochloride (Original Application) as a generic version of diltiazem hydrochloride.

• FDA approval · 2023-02-21
  FDA Approved: PROPAFENONE HYDROCHLORIDE — Original Application (Aurobindo Pharma Limited)

  FDA approved a generic Propafenone hydrochloride product from Aurobindo Pharma Limited under an Original Application. This marks market entr…

• FDA approval · 2022-12-13
  FDA Approved: ESMOLOL HYDROCHLORIDE — Original Application (Amneal Pharmaceuticals LLC)

  FDA approved Amneal Pharmaceuticals' Esmolol hydrochloride in sodium chloride as a generic injectable under an Original Application (ANDA).

• FDA approval · 2022-12-02
  FDA Approved: ESMOLOL HYDROCHLORIDE — Original Application (WG Critical Care, LLC)

  FDA approved the original application for esmolol hydrochloride in saline (sodium chloride) solution, a generic injectable beta-blocker.

• FDA approval · 2022-08-08
  FDA Approved: DILTIAZEM HYDROCHLORIDE — Original Application (Slate Run Pharmaceuticals, LLC)

  FDA approved Slate Run Pharmaceuticals' generic diltiazem hydrochloride under an original ANDA.

• FDA approval · 2022-06-15
  FDA Approved: VERAPAMIL HYDROCHLORIDE — Original Application (Lifestar Pharma LLC)

  FDA approves a generic Verapamil Hydrochloride product from Lifestar Pharma LLC under an Original Application (ANDA).