NDC 62756-377 – Omeprazole
Omeprazole 20 mg/1 · Tablet, Delayed Release · Oral
Product NDC62756-377
Product details
- Brand name
- Omeprazole
- Generic name
- Omeprazole
- Labeler
- Sun Pharmaceutical Industries, Inc.
- Dosage form
- Tablet, Delayed Release
- Route
- Oral
- Marketing category
- ANDA · ANDA207891
- Marketed since
- January 1, 2019
- Listing expires
- December 31, 2026
- Pharmacologic class
- Proton Pump Inhibitor
Active ingredients
- Omeprazole 20 mg/1
Package NDC codes (6)
| Package NDC | Description | Since |
|---|---|---|
| 62756-377-11 | 2 BOTTLE in 1 CARTON (62756-377-11) / 14 TABLET, DELAYED RELEASE in 1 BOTTLE | Jan 1, 2019 |
| 62756-377-12 | 3 BOTTLE in 1 CARTON (62756-377-12) / 14 TABLET, DELAYED RELEASE in 1 BOTTLE | Jan 1, 2019 |
| 62756-377-21 | 1 BOTTLE in 1 CARTON (62756-377-21) / 14 TABLET, DELAYED RELEASE in 1 BOTTLE | Jan 1, 2019 |
| 62756-377-70 | 1 BLISTER PACK in 1 CARTON (62756-377-70) / 14 TABLET, DELAYED RELEASE in 1 BLISTER PACK | Jan 1, 2019 |
| 62756-377-79 | 3 BLISTER PACK in 1 CARTON (62756-377-79) / 14 TABLET, DELAYED RELEASE in 1 BLISTER PACK | Jan 1, 2019 |
| 62756-377-96 | 2 BLISTER PACK in 1 CARTON (62756-377-96) / 14 TABLET, DELAYED RELEASE in 1 BLISTER PACK | Jan 1, 2019 |
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