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FDA label_change · 2014-12-31

FDA Approved: LOTREL — Supplemental Application (Novartis Pharmaceuticals Corporation)

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Summary

FDA approved a supplemental application for Lotrel (amlodipine besylate and benazepril hydrochloride) submitted by Novartis Pharmaceuticals Corporation.

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Diseases / indications

Drugs mentioned

  • LOTREL (amlodipine besylate and benazepril hydrochloride)

Snippet

SUPPL AP for LOTREL (AMLODIPINE BESYLATE AND BENAZEPRIL HYDROCHLORIDE)