🇺🇸 TRICHLORMETHIAZIDE in United States

FDA authorised TRICHLORMETHIAZIDE on 9 March 1960

Marketing authorisations

FDA — authorised 9 March 1960

  • Application: NDA012265
  • Marketing authorisation holder: SCHERING
  • Local brand name: NAQUA
  • Indication: TABLET — ORAL
  • Status: approved

Read official source →

FDA — authorised 16 May 1977

  • Application: ANDA085630
  • Marketing authorisation holder: LANNETT
  • Local brand name: TRICHLOREX
  • Indication: TABLET — ORAL
  • Status: approved

Read official source →

FDA — authorised 5 October 1977

  • Application: ANDA085568
  • Marketing authorisation holder: CHARTWELL RX
  • Local brand name: TRICHLORMETHIAZIDE
  • Indication: TABLET — ORAL
  • Status: approved

Read official source →

FDA — authorised 31 October 1978

  • Application: ANDA086458
  • Marketing authorisation holder: WATSON LABS
  • Local brand name: TRICHLORMETHIAZIDE
  • Indication: TABLET — ORAL
  • Status: approved

Read official source →

FDA — authorised 11 August 1980

  • Application: ANDA083436
  • Marketing authorisation holder: LANNETT
  • Local brand name: TRICHLOREX
  • Indication: TABLET — ORAL
  • Status: approved

Read official source →

FDA — authorised 21 July 1982

  • Application: ANDA086171
  • Marketing authorisation holder: SANDOZ
  • Local brand name: TRICHLORMETHIAZIDE
  • Indication: TABLET — ORAL
  • Status: approved

Read official source →

FDA — authorised 16 June 1988

  • Application: NDA012594
  • Marketing authorisation holder: SANOFI AVENTIS US
  • Local brand name: METAHYDRIN
  • Indication: TABLET — ORAL
  • Status: approved

Read official source →

FDA

  • Application: ANDA083462
  • Marketing authorisation holder: WATSON LABS
  • Local brand name: TRICHLORMETHIAZIDE
  • Indication: TABLET — ORAL
  • Status: approved

Read official source →

FDA

  • Application: ANDA083967
  • Marketing authorisation holder: IMPAX LABS
  • Local brand name: TRICHLORMETHIAZIDE
  • Indication: TABLET — ORAL
  • Status: approved

Read official source →

FDA

  • Status: approved

FDA

  • Application: ANDA085962
  • Marketing authorisation holder: WATSON LABS
  • Local brand name: TRICHLORMETHIAZIDE
  • Indication: TABLET — ORAL
  • Status: approved

Read official source →

TRICHLORMETHIAZIDE in other countries

Same drug, different regulators. Each page below lists the local marketing authorisation, HTA position, pricing, and adverse-event data.

Frequently asked questions

Is TRICHLORMETHIAZIDE approved in United States?

Yes. FDA authorised it on 9 March 1960; FDA authorised it on 16 May 1977; FDA authorised it on 5 October 1977.

Who is the marketing authorisation holder for TRICHLORMETHIAZIDE in United States?

SCHERING holds the US marketing authorisation.