ANDA 80500, held by Solvay. Rauwolfia Serpentina Root.
As of Nov 15, 2026, ANDA 80500 (Rauwolfia Serpentina), held by Solvay, was first approved by FDA on Jul 11, 1972, with 0 approved supplements and 0 published complete response letters.
| Date | Submission | Status | Documents |
|---|---|---|---|
| Jul 11, 1972 | Original application | Approved | None posted |
| Rauwolfia Serpentina50MG · tablet;oral | Rauwolfia Serpentina Root | Discontinued |
| Rauwolfia Serpentina100MG · tablet;oral | Rauwolfia Serpentina Root | 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
