NDC 82009-022 – Omeprazole
Omeprazole 20 mg/1 · Capsule, Delayed Release · Oral
Product NDC82009-022
Product details
- Brand name
- Omeprazole
- Generic name
- Omeprazole
- Labeler
- Quallent Pharmaceuticals Health LLC
- Dosage form
- Capsule, Delayed Release
- Route
- Oral
- Marketing category
- ANDA · ANDA075576
- Marketed since
- November 15, 2022
- Marketing end
- August 30, 2028
- Pharmacologic class
- Proton Pump Inhibitor
Active ingredients
- Omeprazole 20 mg/1
Package NDC codes (1)
| Package NDC | Description | Since |
|---|---|---|
| 82009-022-10 | 1000 CAPSULE, DELAYED RELEASE in 1 BOTTLE (82009-022-10) | Nov 15, 2022 |
Recalls mentioning this NDC
- D-0525-2025 Jul 23, 2025 · Class II
Presence of foreign tablets/capsules: presence of foreign Divalproex Sodium Extended-Release 250mg tablet in a bottle of omeprazole capsules.
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