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FDA Approval Activities for this Drug…
Aciphex (Rabeprazole Sodium) Delayed-Release Tablets, Eisai NDA 20-973/S16 8/1/03 8/15/03 Aciphex (Rabeprazole Sodium) Delayed-Release Tablets, Eisai NDA 20-973/S15 9/30/02 10/2/02 Aciphex (Rabeprazole Sodium) Delayed-Release Tablets, Eisai NDA 20-973/S14 9/23/02 9/27/02 ACIPHEX (rabeprazole sodium) Delayed-Release Tablets, 20 mg. Eisai Medical Research NDA 21-456 NDA 20-973/S-013 11/8/02 11/18/02 11/8/02 4/25/03 Aciphex (Rabeprazole Sodium) Delayed-Release Tablets, Eisai NDA 20-973/S12 5/29/02 6/3/02 Aciphex (Rabeprazole Sodium) Delayed-Release Tablets, Eisai NDA 20-973/S9 2/12/02 2/21/02 2/21/02 Aciphex (Rabeprazole Sodium) Delayed-Release Tablets, Eisai NDA 20-973/S8 08/15/01 04/25/03 Aciphex (Rabeprazole Sodium) Delayed-Release Tablets, Eisai NDA 20-973 | Aciphex (rabeprazole sodium) Delayed-Release Tablets, Eisai Medical, Labeling Revision | Rabeprazole Sodium Delayed Release, Mylan Pharma, Tentative Approval | Rabeprazole Sodium Delayed Release Tablets, Teva Pharmaceuticals, Tentative Approval | Rabeprazole Sodium Delayed-release Tablets, Teva Pharma, Approval
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