NDC 51660-029 – Omeprazole
Omeprazole 20 mg/1 · Tablet, Delayed Release · Oral
Product NDC51660-029
Product details
- Brand name
- Omeprazole
- Generic name
- Omeprazole
- Labeler
- OHM LABORATORIES INC.
- Dosage form
- Tablet, Delayed Release
- Route
- Oral
- Marketing category
- ANDA · ANDA207891
- Marketed since
- June 1, 2019
- Listing expires
- December 31, 2026
- Pharmacologic class
- Proton Pump Inhibitor
Active ingredients
- Omeprazole 20 mg/1
Package NDC codes (3)
| Package NDC | Description | Since |
|---|---|---|
| 51660-029-14 | 1 BOTTLE in 1 CARTON (51660-029-14) / 14 TABLET, DELAYED RELEASE in 1 BOTTLE | Jun 1, 2019 |
| 51660-029-27 | 2 BOTTLE in 1 CARTON (51660-029-27) / 14 TABLET, DELAYED RELEASE in 1 BOTTLE | Jun 1, 2019 |
| 51660-029-44 | 3 BOTTLE in 1 CARTON (51660-029-44) / 14 TABLET, DELAYED RELEASE in 1 BOTTLE | Jun 1, 2019 |
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