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Treats seizures associated with Lennox-Gastaut syndrome (LGS). ANDA 210978, held by Taro. Clobazam.
As of Nov 15, 2026, ANDA 210978 (Clobazam), held by Taro, was first approved by FDA on Apr 15, 2019, with 2 approved supplements and 0 published complete response letters.
First approved: Apr 15, 2019
Review: Standard
Supplements approved: 2
Complete response letters: 0
What It's For
From the FDA-approved label (Indications and Usage)
Clobazam oral suspension is indicated for the adjunctive treatment of seizures associated with Lennox-Gastaut syndrome (LGS) in patients 2 years of age or older. Clobazam is a benzodiazepine indicated for adjunctive treatment of seizures associated with Lennox-Gastaut syndrome (LGS) in patients 2 years of age or older
Approvals, supplements, products and documents come from FDA's Drugs@FDA data files, refreshed daily; Drugs@FDA lists approved applications only. Complete response letters are FDA's published letters.Drugs@FDA and FDA complete response letters