Treats active duodenal ulcer. ANDA 77314, held by Dr Reddys Labs Ltd. Nizatidine.
As of Nov 15, 2026, ANDA 77314 (Nizatidine), held by Dr Reddys Labs Ltd, was first approved by FDA on Sep 15, 2005, with 0 approved supplements and 0 published complete response letters.
INDICATIONS AND USAGE Nizatidine capsules are indicated for up to 8 weeks for the treatment of active duodenal ulcer. In most patients, the ulcer will heal within 4 weeks. Nizatidine capsules are indicated for maintenance therapy for duodenal ulcer patients at a reduced dosage of 150 mg h.s. after healing of an active duodenal ulcer. The consequences of continuous therapy with nizatidine for longer than 1 year are not known. Nizatidine capsules are indicated for up to 12 weeks for the treatment of endoscopically diagnosed esophagitis, including erosive and ulcerative esophagitis, and associated heartburn due to GERD. Nizatidine capsules are
| Date | Submission | Status | Documents |
|---|---|---|---|
| Sep 15, 2005 | Original application | Approved | None posted |
| Nizatidine150MG · capsule;oral | Nizatidine | Rx |
| Nizatidine300MG · capsule;oral | Nizatidine | Rx |
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
