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FDA label_change · 2009-08-31

FDA Approved: BENAZEPRIL HYDROCHLORIDE AND HYDROCHLOROTHIAZIDE — Supplemental Application (Sandoz Inc)

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Summary

FDA approved a supplemental application for Sandoz Inc.'s benazepril hydrochloride and hydrochlorothiazide fixed-dose combination (ANDA 076631).

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Diseases / indications

Drugs mentioned

  • Benazepril hydrochloride and hydrochlorothiazide (Benazepril hydrochloride and hydrochlorothiazide)

Snippet

SUPPL AP for BENAZEPRIL HYDROCHLORIDE AND HYDROCHLOROTHIAZIDE (BENAZEPRIL HYDROCHLORIDE AND HYDROCHLOROTHIAZIDE)