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# Sun Pharma Not Withdrawing Benazepril HCl/Hydrochlorothiazide
- URL: https://www.fdaweb.com/sun-pharma-not-withdrawing-benazepril-hcl-hydrochlorothiazide/
- Published: 2018-06-06T12:00:00.000Z
- Updated: 2026-09-15T00:11:08.000Z
- Author: David McFarland
- Tags: FDA Policy/General, #legacy-id-D5141617

*Federal Register* notice: FDA is correcting a 2/23 notice that announced the withdrawal of 24 ANDAs from multiple applicants. That notice wrongly stated that Sun Pharmaceutical Industries asked to withdraw ANDA 077483 for benazepril hydrochloride and hydrochlorothiazide tablets, 5 mg/6.25 mg, 10 mg/12.5 mg, 20 mg/12.5 mg, and 20 mg/25 mg. Sun had earlier informed FDA that it did not want approval of the ANDA withdrawn. To view the notice, click [here](https://s3.amazonaws.com/public-inspection.federalregister.gov/2018-12220.pdf?ref=fdaweb.com).