ANDA 83767, held by Watson Labs. Prednisolone Acetate.
As of Nov 15, 2026, ANDA 83767 (Prednisolone Acetate), held by Watson Labs, was not approved, with 0 approved supplements and 0 published complete response letters.
| Product | Active ingredient | Marketing |
|---|---|---|
| Prednisolone Acetate40MG/ML ยท injectable;injection | Prednisolone Acetate | 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
