Details for New Drug Application (NDA): 211390
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The generic ingredient in ZILEUTON is zileuton. There is one drug master file entry for this compound. Six suppliers are listed for this compound. Additional details are available on the zileuton profile page.
Profile for product number 001
| Active Rx/OTC/Discontinued: | RX | Dosage: | TABLET, EXTENDED RELEASE;ORAL | Strength | 600MG | ||||
| Approval Date: | Oct 23, 2020 | TE: | AB | RLD: | No | ||||
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