🇺🇸 best medical care in United States

FDA authorised best medical care on 18 July 1974

Marketing authorisations

FDA — authorised 18 July 1974

  • Application: ANDA083320
  • Marketing authorisation holder: ALRA
  • Local brand name: ACETAZOLAMIDE
  • Indication: TABLET — ORAL
  • Status: approved

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FDA — authorised 31 March 1978

  • Application: ANDA084840
  • Marketing authorisation holder: CHARTWELL MOLECULAR
  • Local brand name: ACETAZOLAMIDE
  • Indication: TABLET — ORAL
  • Status: approved

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FDA — authorised 5 February 1982

  • Application: ANDA087654
  • Marketing authorisation holder: VANGARD
  • Local brand name: ACETAZOLAMIDE
  • Indication: TABLET — ORAL
  • Status: approved

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FDA — authorised 22 October 1985

  • Application: ANDA088882
  • Marketing authorisation holder: HERITAGE PHARMA
  • Local brand name: ACETAZOLAMIDE
  • Indication: TABLET — ORAL
  • Status: approved

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FDA — authorised 22 June 1988

  • Application: ANDA089753
  • Marketing authorisation holder: SUN PHARM INDUSTRIES
  • Local brand name: ACETAZOLAMIDE
  • Indication: TABLET — ORAL
  • Status: approved

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FDA — authorised 10 December 2008

  • Application: ANDA040904
  • Marketing authorisation holder: HERITAGE PHARMA
  • Local brand name: ACETAZOLAMIDE
  • Indication: CAPSULE, EXTENDED RELEASE — ORAL
  • Status: approved

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FDA — authorised 14 July 2011

  • Application: ANDA090779
  • Marketing authorisation holder: INDICUS PHARMA
  • Local brand name: ACETAZOLAMIDE
  • Indication: CAPSULE, EXTENDED RELEASE — ORAL
  • Status: approved

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FDA — authorised 29 March 2016

  • Application: ANDA204691
  • Marketing authorisation holder: MPP PHARMA
  • Local brand name: ACETAZOLAMIDE
  • Indication: CAPSULE, EXTENDED RELEASE — ORAL
  • Status: approved

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FDA — authorised 30 September 2016

  • Application: ANDA203434
  • Marketing authorisation holder: NOVAST LABS
  • Local brand name: ACETAZOLAMIDE
  • Indication: CAPSULE, EXTENDED RELEASE — ORAL
  • Status: approved

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FDA — authorised 27 October 2016

  • Application: ANDA205530
  • Marketing authorisation holder: HERITAGE PHARMA
  • Local brand name: ACETAZOLAMIDE
  • Indication: TABLET — ORAL
  • Status: approved

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FDA — authorised 20 November 2017

  • Application: ANDA209734
  • Marketing authorisation holder: STRIDES PHARMA
  • Local brand name: ACETAZOLAMIDE
  • Indication: TABLET — ORAL
  • Status: approved

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FDA — authorised 18 October 2018

  • Application: ANDA207659
  • Marketing authorisation holder: ACCORD HLTHCARE
  • Local brand name: ACETAZOLAMIDE
  • Indication: CAPSULE, EXTENDED RELEASE — ORAL
  • Status: approved

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FDA — authorised 16 January 2019

  • Application: ANDA205301
  • Marketing authorisation holder: CADILA
  • Local brand name: ACETAZOLAMIDE
  • Indication: CAPSULE, EXTENDED RELEASE — ORAL
  • Status: approved

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FDA — authorised 19 February 2019

  • Application: ANDA210423
  • Marketing authorisation holder: ALEMBIC
  • Local brand name: ACETAZOLAMIDE
  • Indication: CAPSULE, EXTENDED RELEASE — ORAL
  • Status: approved

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FDA — authorised 18 June 2019

  • Application: ANDA203917
  • Marketing authorisation holder: RISING
  • Local brand name: ACETAZOLAMIDE
  • Indication: CAPSULE, EXTENDED RELEASE — ORAL
  • Status: approved

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FDA — authorised 17 October 2019

  • Application: ANDA210588
  • Marketing authorisation holder: NOVITIUM PHARMA
  • Local brand name: ACETAZOLAMIDE
  • Indication: TABLET — ORAL
  • Status: approved

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FDA — authorised 18 October 2019

  • Application: ANDA211556
  • Marketing authorisation holder: HIBROW HLTHCARE
  • Local brand name: ACETAZOLAMIDE
  • Indication: TABLET — ORAL
  • Status: approved

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FDA — authorised 30 April 2020

  • Application: ANDA207503
  • Marketing authorisation holder: BRECKENRIDGE
  • Local brand name: ACETAZOLAMIDE
  • Indication: TABLET — ORAL
  • Status: approved

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FDA — authorised 22 February 2021

  • Application: ANDA211372
  • Marketing authorisation holder: SOMERSET THERAPS LLC
  • Local brand name: ACETAZOLAMIDE
  • Indication: TABLET — ORAL
  • Status: approved

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FDA — authorised 19 August 2021

  • Application: ANDA215101
  • Marketing authorisation holder: RUBICON RESEARCH
  • Local brand name: ACETAZOLAMIDE
  • Indication: TABLET — ORAL
  • Status: approved

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FDA — authorised 4 April 2023

  • Application: ANDA211069
  • Marketing authorisation holder: ZYDUS LIFESCIENCES
  • Local brand name: ACETAZOLAMIDE
  • Indication: TABLET — ORAL
  • Status: approved

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FDA — authorised 9 May 2023

  • Application: ANDA217197
  • Marketing authorisation holder: NE RX PHARMA
  • Local brand name: ACETAZOLAMIDE
  • Indication: TABLET — ORAL
  • Status: approved

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FDA — authorised 11 September 2023

  • Application: ANDA211151
  • Marketing authorisation holder: AJANTA PHARMA LTD
  • Local brand name: ACETAZOLAMIDE
  • Indication: TABLET — ORAL
  • Status: approved

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FDA — authorised 26 January 2024

  • Application: ANDA213706
  • Marketing authorisation holder: TORRENT
  • Local brand name: ACETAZOLAMIDE
  • Indication: TABLET — ORAL
  • Status: approved

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FDA — authorised 14 May 2024

  • Application: ANDA218023
  • Marketing authorisation holder: EPIC PHARMA LLC
  • Local brand name: ACETAZOLAMIDE
  • Indication: TABLET — ORAL
  • Status: approved

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FDA — authorised 30 May 2025

  • Application: ANDA212089
  • Marketing authorisation holder: AUROBINDO PHARMA LTD
  • Local brand name: ACETAZOLAMIDE
  • Indication: TABLET — ORAL
  • Status: approved

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FDA

  • Application: ANDA087686
  • Marketing authorisation holder: ASCOT
  • Local brand name: ACETAZOLAMIDE
  • Indication: TABLET — ORAL
  • Status: approved

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FDA

  • Application: ANDA084498
  • Marketing authorisation holder: WATSON LABS
  • Local brand name: ACETAZOLAMIDE
  • Indication: TABLET — ORAL
  • Status: approved

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Frequently asked questions

Is best medical care approved in United States?

Yes. FDA authorised it on 18 July 1974; FDA authorised it on 31 March 1978; FDA authorised it on 5 February 1982.

Who is the marketing authorisation holder for best medical care in United States?

ALRA holds the US marketing authorisation.