ANDA 75650, held by Actavis Elizabeth. Famotidine.
As of Nov 15, 2026, ANDA 75650 (Famotidine), held by Actavis Elizabeth, was first approved by FDA on Sep 14, 2001, with 2 approved supplements and 0 published complete response letters.
| Date | Submission | Status | Documents |
|---|---|---|---|
| Sep 14, 2001 | Original application | Approved |
| Famotidine20MG · tablet;oral | Famotidine | Discontinued |
| Famotidine40MG · tablet;oral | Famotidine | Discontinued |
| Apr 23, 2002 | Supplement 1Manufacturing | Approved | None posted |
| Jan 7, 2002 | Supplement 2Manufacturing | Approved | None posted |
| Sep 14, 2001 | Original application | Approved |
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
