NDC 46122-739 – Omeprazole
Omeprazole 20 mg/1 · Tablet, Delayed Release · Oral
Product NDC46122-739
Product details
- Brand name
- Omeprazole
- Generic name
- Omeprazole
- Labeler
- AMERISOURCEBERGEN DRUG CORPORATION
- Dosage form
- Tablet, Delayed Release
- Route
- Oral
- Marketing category
- ANDA · ANDA207740
- Marketed since
- November 6, 2018
- Marketing end
- March 31, 2027
- Pharmacologic class
- Proton Pump Inhibitor
Active ingredients
- Omeprazole 20 mg/1
Package NDC codes (2)
| Package NDC | Description | Since |
|---|---|---|
| 46122-739-04 | 3 BOTTLE in 1 CARTON (46122-739-04) / 14 TABLET, DELAYED RELEASE in 1 BOTTLE | Aug 30, 2023 |
| 46122-739-74 | 1 BOTTLE in 1 CARTON (46122-739-74) / 14 TABLET, DELAYED RELEASE in 1 BOTTLE | Aug 30, 2023 |
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