NDC 37835-001 – Omeprazole
Omeprazole 20 mg/1 · Tablet, Delayed Release · Oral
Product NDC37835-001
Product details
- Brand name
- Omeprazole
- Generic name
- Omeprazole
- Labeler
- BI-MART
- Dosage form
- Tablet, Delayed Release
- Route
- Oral
- Marketing category
- ANDA · ANDA207891
- Marketed since
- September 30, 2019
- Listing expires
- December 31, 2026
- Pharmacologic class
- Proton Pump Inhibitor
Active ingredients
- Omeprazole 20 mg/1
Package NDC codes (2)
| Package NDC | Description | Since |
|---|---|---|
| 37835-001-14 | 1 BOTTLE in 1 CARTON (37835-001-14) / 14 TABLET, DELAYED RELEASE in 1 BOTTLE | Sep 30, 2019 |
| 37835-001-42 | 3 BOTTLE in 1 CARTON (37835-001-42) / 14 TABLET, DELAYED RELEASE in 1 BOTTLE | Sep 30, 2019 |
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