NDC 37808-915 – Omeprazole
Omeprazole 20 mg/1 · Tablet, Delayed Release · Oral
Product NDC37808-915
Product details
- Brand name
- Omeprazole
- Generic name
- Omeprazole
- Labeler
- H E B
- Dosage form
- Tablet, Delayed Release
- Route
- Oral
- Marketing category
- NDA · NDA022032
- Marketed since
- February 29, 2008
- Listing expires
- December 31, 2026
- Pharmacologic class
- Proton Pump Inhibitor
Active ingredients
- Omeprazole 20 mg/1
Package NDC codes (3)
| Package NDC | Description | Since |
|---|---|---|
| 37808-915-01 | 1 BOTTLE in 1 CARTON (37808-915-01) / 14 TABLET, DELAYED RELEASE in 1 BOTTLE | Feb 4, 2011 |
| 37808-915-03 | 3 BOTTLE in 1 CARTON (37808-915-03) / 14 TABLET, DELAYED RELEASE in 1 BOTTLE | Apr 27, 2021 |
| 37808-915-30 | 2 CARTON in 1 CARTON (37808-915-30) / 14 BLISTER PACK in 1 CARTON / 1 TABLET, DELAYED RELEASE in 1 BLISTER PACK | Feb 29, 2008 |
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