NDC 43598-561 – Lansoprazole
Lansoprazole 30 mg/1 · Tablet, Orally Disintegrating, Delayed Release · Oral
Product NDC43598-561
Product details
- Brand name
- Lansoprazole
- Generic name
- Lansoprazole
- Labeler
- Dr.Reddys Laboratories Inc
- Dosage form
- Tablet, Orally Disintegrating, Delayed Release
- Route
- Oral
- Marketing category
- ANDA · ANDA210465
- Marketed since
- February 1, 2021
- Marketing end
- September 30, 2026
- Pharmacologic class
- Proton Pump Inhibitor
Active ingredients
- Lansoprazole 30 mg/1
Package NDC codes (1)
| Package NDC | Description | Since |
|---|---|---|
| 43598-561-78 | 100 BLISTER PACK in 1 CARTON (43598-561-78) / 10 TABLET, ORALLY DISINTEGRATING, DELAYED RELEASE in 1 BLISTER PACK (43598-561-79) | Feb 1, 2021 |
Recalls mentioning this NDC
- D-1288-2022 Aug 3, 2022 · Class II
FAILED DISSOLUTION SPECIFICATIONS - D-1287-2022 Aug 3, 2022 · Class II
FAILED DISSOLUTION SPECIFICATIONS - D-0853-2022 May 11, 2022 · Class II
Failed Dissolution Specifications
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