NDC 41163-915 – Equaline omeprazole
Omeprazole 20 mg/1 · Tablet, Delayed Release · Oral
Product NDC41163-915
Product details
- Brand name
- Equaline omeprazole
- Generic name
- Omeprazole
- Labeler
- United Natural Foods, Inc. dba UNFI
- Dosage form
- Tablet, Delayed Release
- Route
- Oral
- Marketing category
- NDA · NDA022032
- Marketed since
- February 22, 2008
- Listing expires
- December 31, 2026
- Pharmacologic class
- Proton Pump Inhibitor
Active ingredients
- Omeprazole 20 mg/1
Uses, dosage, side effects and warnings for Equaline omeprazole →
Package NDC codes (4)
| Package NDC | Description | Since |
|---|---|---|
| 41163-915-01 | 1 BOTTLE in 1 CARTON (41163-915-01) / 14 TABLET, DELAYED RELEASE in 1 BOTTLE | Sep 27, 2011 |
| 41163-915-30 | 2 CARTON in 1 CARTON (41163-915-30) / 14 BLISTER PACK in 1 CARTON / 1 TABLET, DELAYED RELEASE in 1 BLISTER PACK | Feb 22, 2008 |
| 41163-915-55 | 3 CARTON in 1 CARTON (41163-915-55) / 14 BLISTER PACK in 1 CARTON / 1 TABLET, DELAYED RELEASE in 1 BLISTER PACK | Feb 25, 2008 |
| 41163-915-74 | 14 BLISTER PACK in 1 CARTON (41163-915-74) / 1 TABLET, DELAYED RELEASE in 1 BLISTER PACK | Feb 22, 2008 |
Other Equaline omeprazole products
- 41163-634 Omeprazole 20 mg/1 · Tablet, Orally Disintegrating, Delayed Release · United Natural Foods, Inc. dba UNFI