NDA 20773, held by Bracco. Simethicone-Cellulose.
As of Nov 13, 2026, NDA 20773 (Sonorx), held by Bracco, was first approved by FDA on Oct 29, 1998, with 0 approved supplements and 0 published complete response letters.
| Date | Submission | Status | Documents |
|---|---|---|---|
| Oct 29, 1998 | Original applicationNew dosage form · Standard review | Approved |
| Product | Active ingredient | Marketing |
|---|---|---|
| Sonorx7.5MG/ML · suspension;oral | Simethicone-Cellulose | Discontinued |
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