NDC 55111-398 – Lansoprazole
Lansoprazole 15 mg/1 · Capsule, Delayed Release · Oral
Product NDC55111-398
Product details
- Brand name
- Lansoprazole
- Generic name
- Lansoprazole
- Labeler
- Dr.Reddy's Laboratories Ltd.
- Dosage form
- Capsule, Delayed Release
- Route
- Oral
- Marketing category
- ANDA · ANDA091269
- Marketed since
- October 15, 2010
- Listing expires
- December 31, 2026
- Pharmacologic class
- Proton Pump Inhibitor
Active ingredients
- Lansoprazole 15 mg/1
Package NDC codes (6)
| Package NDC | Description | Since |
|---|---|---|
| 55111-398-01 | 100 CAPSULE, DELAYED RELEASE in 1 BOTTLE (55111-398-01) | Oct 15, 2010 |
| 55111-398-05 | 500 CAPSULE, DELAYED RELEASE in 1 BOTTLE (55111-398-05) | Oct 15, 2010 |
| 55111-398-30 | 30 CAPSULE, DELAYED RELEASE in 1 BOTTLE (55111-398-30) | Oct 15, 2010 |
| 55111-398-60 | 60 CAPSULE, DELAYED RELEASE in 1 BOTTLE (55111-398-60) | Oct 15, 2010 |
| 55111-398-79 | 1 BLISTER PACK in 1 CARTON (55111-398-79) / 10 CAPSULE, DELAYED RELEASE in 1 BLISTER PACK | Oct 15, 2010 |
| 55111-398-90 | 90 CAPSULE, DELAYED RELEASE in 1 BOTTLE (55111-398-90) | Oct 15, 2010 |
Recalls mentioning this NDC
- D-0737-2022 Apr 6, 2022 · Class II
Failed Dissolution Specifications; during long term stability testing. - D-0738-2022 Apr 6, 2022 · Class II
Failed Dissolution Specifications; during long term stability testing.
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