NDC 68001-441 – Omeprazole
Omeprazole 20 mg/1 · Tablet, Delayed Release · Oral
Product NDC68001-441
Product details
- Brand name
- Omeprazole
- Generic name
- Omeprazole
- Labeler
- BluePoint Laboratories
- Dosage form
- Tablet, Delayed Release
- Route
- Oral
- Marketing category
- ANDA · ANDA207740
- Marketed since
- June 19, 2020
- Listing expires
- December 31, 2026
- Pharmacologic class
- Proton Pump Inhibitor
Active ingredients
- Omeprazole 20 mg/1
Package NDC codes (3)
| Package NDC | Description | Since |
|---|---|---|
| 68001-441-39 | 2 BOTTLE in 1 CARTON (68001-441-39) / 14 TABLET, DELAYED RELEASE in 1 BOTTLE (68001-441-55) | Jun 19, 2020 |
| 68001-441-40 | 3 BOTTLE in 1 CARTON (68001-441-40) / 14 TABLET, DELAYED RELEASE in 1 BOTTLE (68001-441-55) | Jun 19, 2020 |
| 68001-441-98 | 1 BOTTLE in 1 CARTON (68001-441-98) / 14 TABLET, DELAYED RELEASE in 1 BOTTLE (68001-441-55) | Jun 19, 2020 |
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