NDC 62175-118 – Omeprazole
Omeprazole 20 mg/1 · Capsule, Delayed Release · Oral
Product NDC62175-118
Product details
- Brand name
- Omeprazole
- Generic name
- Omeprazole
- Labeler
- Lannett Company, Inc.
- Dosage form
- Capsule, Delayed Release
- Route
- Oral
- Marketing category
- ANDA · ANDA075410
- Marketed since
- November 4, 2002
- Listing expires
- December 31, 2026
- Pharmacologic class
- Proton Pump Inhibitor
Active ingredients
- Omeprazole 20 mg/1
Package NDC codes (5)
| Package NDC | Description | Since |
|---|---|---|
| 62175-118-32 | 30 CAPSULE, DELAYED RELEASE in 1 BOTTLE (62175-118-32) | Nov 4, 2002 |
| 62175-118-37 | 100 CAPSULE, DELAYED RELEASE in 1 BOTTLE (62175-118-37) | Nov 4, 2002 |
| 62175-118-43 | 1000 CAPSULE, DELAYED RELEASE in 1 BOTTLE (62175-118-43) | Nov 4, 2002 |
| 62175-118-46 | 90 CAPSULE, DELAYED RELEASE in 1 BOTTLE (62175-118-46) | Nov 4, 2002 |
| 62175-118-49 | 54000 CAPSULE, DELAYED RELEASE in 1 DRUM (62175-118-49) | Nov 4, 2002 |
Recalls mentioning this NDC
- D-009-2014 Nov 27, 2013 · Class II
Failed Tablet/Capsule Specification: some capsules over time do not meet or are suspected to not meet the specification for acid resistance.
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