NDC 37808-569 – Omeprazole Delayed-Release
Omeprazole Magnesium 20 mg/1 · Tablet, Delayed Release · Oral
Product NDC37808-569
Product details
- Brand name
- Omeprazole Delayed-Release
- Generic name
- Omeprazole
- Labeler
- H-E-B
- Dosage form
- Tablet, Delayed Release
- Route
- Oral
- Marketing category
- ANDA · ANDA218829
- Marketed since
- July 1, 2026
- Listing expires
- December 31, 2027
- Pharmacologic class
- Proton Pump Inhibitor
Active ingredients
- Omeprazole Magnesium 20 mg/1
Uses, dosage, side effects and warnings for Omeprazole Delayed-Release →
Package NDC codes (3)
| Package NDC | Description | Since |
|---|---|---|
| 37808-569-41 | 3 BOTTLE in 1 CARTON (37808-569-41) / 14 TABLET, DELAYED RELEASE in 1 BOTTLE | Jul 1, 2026 |
| 37808-569-45 | 1 BOTTLE in 1 CARTON (37808-569-45) / 14 TABLET, DELAYED RELEASE in 1 BOTTLE | Jul 1, 2026 |
| 37808-569-82 | 2 BOTTLE in 1 CARTON (37808-569-82) / 14 TABLET, DELAYED RELEASE in 1 BOTTLE | Jul 1, 2026 |
Other Omeprazole Delayed-Release products
- 49483-731 Omeprazole Magnesium 20 mg/1 · Tablet, Delayed Release · TIME CAP LABORATORIES, INC.